#Veterinary Therapeutics Market

[adhk1234]

Veterinary Therapeutics Market: SWOT Analysis and Market Positioning

The global veterinary therapeutics market is experiencing significant growth, driven by rising awareness of animal health, advancements in veterinary medicine, and the increasing prevalence of animal diseases. Valued at USD 43.58 billion in 2023, the market is projected to reach USD 82.40 billion by 2032, exhibiting a compound annual growth rate (CAGR) of 7.35% from 2024 to 2032.

Market Segmentation:

The veterinary therapeutics market is segmented based on type and application:

By Type:

Anti-Inflammatory Drugs

Parasiticides

Others

By Application:

Hospitals

Veterinary Clinics

Drug Stores

Others

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Regional Analysis:

North America: Leading the market due to high pet ownership rates and advanced veterinary healthcare infrastructure.

Europe: Significant growth driven by increased awareness of animal health and welfare.

Asia-Pacific: Expected to witness rapid growth owing to rising disposable incomes and increasing pet adoption rates.

Key Players and Their Products in the Veterinary Therapeutics Market

Zoetis, Inc. - Apoquel (allergy treatment), Simparica Trio (flea, tick, and heartworm protection), Rimadyl (pain relief), Convenia (antibiotics), Vanguard vaccines.

Intervet Inc. (Merck Animal Health) - Nobivac vaccines (for dogs and cats), Banamine (pain relief), Safe-Guard (antiparasitic), Zuprevo (respiratory disease treatment), Revalor (growth implants).

Elanco Animal Health - Trifexis (flea, heartworm, intestinal parasite control), Galliprant (pain and inflammation relief), Cydectin (antiparasitic), Inteprity (poultry gut health management).

Merial (Acquired by Boehringer Ingelheim) - Frontline (flea and tick prevention), Heartgard (heartworm disease prevention), Purevax vaccines (cats).

Bayer AG (Now part of Elanco Animal Health) - Advantix (flea and tick treatment), Baytril (antibiotics), Profender (dewormer).

Boehringer Ingelheim International GmbH - NexGard (flea and tick control), Ingelvac (swine vaccines), Duramune (canine vaccines), Metacam (pain relief).

Ceva Santé Animale - Vectra (flea and tick treatment), Cevac vaccines (for poultry), Adaptil (stress management in dogs), Feliway (cat pheromone product).

Vetoquinol S.A. - Marbocyl (antibiotics), Clavaseptin (antimicrobial), Vetprofen (pain management), Zylkene (behavior support).

IDEXX Laboratories, Inc. - SNAP diagnostics (rapid tests for diseases like parvovirus and heartworm), Cornerstone software (veterinary practice management).

Virbac - Effipro (flea and tick protection), CaniLeish (leishmaniasis vaccine), Milpro (broad-spectrum dewormer).

Biogénesis Bagó SA - BioBos vaccines (for livestock), Suigen vaccines (swine health), MasterVet antibiotics.

Biovac Ltd. - Vaccines for poultry and livestock diseases like Newcastle disease and foot-and-mouth disease.

Key Highlights:

Advancements in veterinary medicine, including the development of monoclonal antibody therapies and controlled-release drug delivery systems, are enhancing treatment efficacy.

The increasing prevalence of chronic and zoonotic diseases underscores the importance of effective veterinary therapeutics.

Growing awareness among pet owners and livestock farmers is driving demand for preventive and therapeutic veterinary care.

Future Outlook:

The veterinary therapeutics market is poised for substantial growth, propelled by continuous innovations in veterinary medicine and a heightened focus on animal health. The development of targeted treatments and advanced diagnostic tools is expected to further enhance the quality of care provided to animals. As awareness of the importance of veterinary health increases globally, the demand for effective therapeutic solutions is anticipated to rise, offering significant opportunities for industry stakeholders.

Conclusion:

The global veterinary therapeutics market is on a robust growth trajectory, with substantial advancements in treatment options and increasing awareness of animal health. Stakeholders, including manufacturers, healthcare providers, and investors, are well-positioned to benefit from the evolving landscape of veterinary therapeutics.

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The Veterinary Therapeutics Market in 2023 is US$ 49.7 billion, and is expected to reach US$ 79.34 billion by 2031 at a CAGR of 6%.

[trendtrackershq]

Gene Editing Revolutionizing Animal Therapeutics and Diagnostics Market: Exploring CRISPR-Cas9 and Its Potential Applications

Introduction:

In recent years, gene editing has emerged as a revolutionary tool in the field of animal health, offering unprecedented precision in treating genetic diseases. Among the various gene editing technologies, CRISPR-Cas9 stands out for its efficiency, versatility, and potential applications in correcting genetic anomalies in animals. In this comprehensive article, we delve into the latest advancements in CRISPR-Cas9 technology and its transformative impact on animal therapeutics.

According to the study by Next Move Strategy Consulting, the global Animal Therapeutics and Diagnostics Market size is predicted to reach USD 59.21 billion with a CAGR of 5.5% by 2030.

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Understanding CRISPR-Cas9:

CRISPR-Cas9, short for Clustered Regularly Interspaced Short Palindromic Repeats and CRISPR-associated protein 9, is a genome editing tool derived from a bacterial defense mechanism. It enables scientists to precisely modify DNA sequences within the genome of an organism. The CRISPR-Cas9 system consists of two key components: a guide RNA (gRNA) that directs the Cas9 enzyme to the target DNA sequence, and the Cas9 enzyme itself, which acts as molecular scissors to cut the DNA at the specified location.

Advancements in CRISPR-Cas9 Technology:

Over the past decade, significant advancements have been made to enhance the efficiency, accuracy, and versatility of CRISPR-Cas9 gene editing. Initially discovered in bacteria as a defense mechanism against viral infections, CRISPR-Cas9 has been adapted for use in a wide range of organisms, including animals. One of the primary challenges in early CRISPR-Cas9 applications was off-target effects, where the Cas9 enzyme could inadvertently cleave DNA sequences similar to the target site, leading to unintended genetic alterations. However, researchers have developed novel strategies to improve the specificity of Cas9, reducing off-target effects and minimizing the risk of unintended mutations.

Several approaches have been employed to enhance the precision of CRISPR-Cas9 gene editing, including the engineering of Cas9 variants with altered DNA-binding properties, the optimization of gRNA design algorithms to improve target specificity, and the development of bioinformatics tools for predicting off-target cleavage sites. Additionally, the implementation of stringent quality control measures and validation protocols has contributed to the reliability and reproducibility of CRISPR-Cas9 experiments.

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Furthermore, the development of base editing and prime editing techniques has expanded the scope of CRISPR-Cas9 applications, allowing for precise nucleotide substitutions and targeted insertions or deletions without double-strand breaks. Base editing involves the direct conversion of one DNA base pair into another, enabling the correction of point mutations associated with genetic diseases. Prime editing, on the other hand, combines CRISPR-Cas9 with a reverse transcriptase enzyme to precisely edit DNA sequences with single-base precision, offering greater flexibility and efficiency in genome engineering.

Potential Applications in Treating Genetic Diseases:

One of the most promising applications of CRISPR-Cas9 in animal health is the treatment of genetic diseases. Inherited disorders, such as muscular dystrophy, cystic fibrosis, and hemophilia, can be debilitating for animals and pose significant challenges for traditional therapeutic approaches. CRISPR-Cas9 offers a targeted solution by enabling precise corrections of disease-causing mutations at the genetic level.

For example, in a groundbreaking study published in 2017, researchers used CRISPR-Cas9 to correct a genetic mutation responsible for Duchenne muscular dystrophy (DMD) in dogs. By delivering the CRISPR components directly into the muscles of affected dogs, the scientists were able to restore dystrophin expression and improve muscle function, offering hope for future therapeutic interventions in human patients with DMD.

Beyond monogenic disorders, CRISPR-Cas9 holds promise for addressing complex polygenic traits and susceptibility to infectious diseases in animals. By editing key genes involved in disease resistance or immune response pathways, researchers aim to develop animals with enhanced resilience to pathogens and reduced susceptibility to common illnesses.

In addition to therapeutic applications, CRISPR-Cas9 can also be utilized for disease modeling and drug discovery in animals. By generating animal models with precise genetic modifications that mimic human diseases, researchers can gain insights into disease mechanisms, identify potential drug targets, and evaluate the efficacy of novel therapeutics in preclinical studies.

Challenges and Considerations:

While the potential of CRISPR-Cas9 in animal therapeutics is immense, several challenges and ethical considerations must be addressed. Off-target effects, unintended genetic modifications, and the potential for germline transmission of edited traits raise concerns about safety and unintended consequences. Although significant progress has been made in improving the specificity and efficiency of CRISPR-Cas9 gene editing, the risk of off-target effects remains a persistent challenge that requires ongoing research and optimization.

Furthermore, the long-term effects of CRISPR-Cas9-mediated genetic modifications on animal health and welfare are still not fully understood. Ethical considerations surrounding the use of gene editing in animals, particularly in the context of agricultural applications and livestock breeding, necessitate careful deliberation and stakeholder engagement. Regulatory frameworks governing the use of gene editing in animals vary across jurisdictions, ranging from strict prohibitions to permissive regulations with stringent oversight requirements.

Conclusion:

In conclusion, CRISPR-Cas9 represents a paradigm shift in the field of animal health, offering unprecedented opportunities for the treatment of genetic diseases and the enhancement of desirable traits in animals. With continued advancements in CRISPR-Cas9 technology and ongoing research efforts, the future holds great promise for harnessing the power of gene editing to improve the health and well-being of animals worldwide. However, it is essential to proceed with caution, ensuring responsible use and thoughtful consideration of the ethical implications associated with gene editing in animals.

Through this comprehensive article, we have explored the latest advancements in CRISPR-Cas9 technology and its potential applications in treating genetic diseases in animals. As researchers continue to push the boundaries of gene editing capabilities, the possibilities for transformative interventions in animal health are limitless. By addressing the challenges and ethical considerations surrounding CRISPR-Cas9 gene editing, we can pave the way for safer, more effective, and ethically sound applications of this groundbreaking technology in veterinary medicine.

[growthofcarsharingmarket]

The global veterinary eye care therapeutics market is estimated at US$ 780-800 million in 2022 and is expected to grow at a significant CAGR of 3.7% over the forecast period of 2022-2030.According to a deep-dive market assessment by RationalStat, the global Veterinary Eye Care Therapeutics market has been analyzed on the basis of market segments, including treatment, indication, animal type, end user, and geography/regions (incl. North America, Latin America, Western Europe, Eastern Europe, Middle East & Africa, and Asia Pacific). The report also offers global and regional market size for 2019-2022 and forecasts 2022-2030.

[mariacallous]

There’s a well-established inverse relationship between a dog’s size and its expected lifespan. Bernese mountain dogs and Great Danes live just six to eight years, for example, while corgis can live up to 15 years and Chihuahuas up to two decades.

San Francisco biotech company Loyal wants to close that gap, and is developing an experimental drug to extend the lifespan and improve the quality of life of large and giant dog breeds. Today, the company announced that based on early data, the US Food and Drug Administration has determined that Loyal’s drug has a “reasonable expectation of effectiveness.” The company hasn’t yet shown that its drug actually extends lifespan, but the FDA decision signals the agency’s confidence in Loyal’s approach, and the drug will soon be tested in a bigger trial.

“Big dog owners want more time with their dogs,” says Loyal CEO Celine Halioua. “It’s really heartbreaking to people that they don’t live that long.” She argues that the wide variety in dog sizes isn’t natural, but a result of selective breeding by humans to create dogs with certain physical traits or that can perform specific tasks. On average, mixed-breed dogs live longer than their purebred counterparts.

So far, the FDA has not approved any drugs to expand the lifespan of animals—or humans, for that matter. “This is completely novel,” says Linda Rhodes, former CEO of pet biotech company Aratana Therapeutics and a consultant for Loyal. It’s difficult to study life-extension drugs in people, she says, because humans live relatively longer lives than other species. But starting with dogs—and the breeds with the shortest lives—could yield important clues. “The implication for other species, including humans, is pretty profound,” she says.

Loyal’s experimental drug is an injection designed to be given every three to six months by a veterinarian. The drug is meant to lower levels of a hormone called IGF-1, which is involved in growth and metabolism and has been linked to dog size. Large dogs have a genetic variant that leads to high levels of IGF-1 and small dogs have a different variant that results in lower levels.

Inhibiting this hormone has been shown to increase lifespan in worms, flies, and rodents. In humans, both very high and very low levels increase mortality risk, while a midrange is associated with the lowest mortality.

In early studies, Loyal dosed 130 research dogs with its investigational drug. Halioua says the company has shown that it can reduce IGF-1 levels in large dogs to those seen in medium-size dogs. Two dogs had loose stools for a day or two after receiving the injection, but beyond that, Halioua says, no major side effects have been observed.

To determine the drug’s effect on lifespan, the company is planning a bigger study that will start in 2024 or 2025, and enroll about 1,000 large and giant breed companion dogs that are at least 7 years old. Each will receive either the experimental drug or a placebo.

Halioua says the company aims to have its drug on the market by 2026. But first, Loyal still has to prove to the FDA—which regulates both human and veterinary medicines—that the injection is safe and that the drug can be reliably manufactured. At that point, the FDA can grant conditional approval, a temporary authorization that lasts five years and allows the drug to be sold by prescription. During that time, Loyal will collect effectiveness data and apply for full approval.

Loyal is also working on two other drugs: a pill version for large and giant dog breeds, and a pill for older dogs of all breeds.

Danika Bannasch, a veterinary geneticist at the University of California, Davis, who specializes in canine genetics, says that IGF-1 is only one factor thought to be associated with dog size and longevity. “As for targeting it, I think it’s a bit premature. We know that smaller breed dogs live longer than larger breed dogs, but we don’t know how much of that is due to the influence of IGF-1,” she says.

In a study published last month, Bannasch and her colleagues identified another possible driver of dog longevity, a gene called ERBB4. Studying more than 300 golden retrievers, they compared the DNA from blood samples of dogs that were still alive at 14 years of age to those that died before age 12. They found that dogs with certain variants of the gene survived longer—on average, 13.5 years compared to 11.6 years. Bannasch cautions that the work was conducted in only one breed and that it’s not known whether these variants are associated with longer life in other types of dogs.

The ERBB4 gene is the canine version of HER4, a human gene closely related to HER2, which is associated with cancer. Studying the canine gene could have implications for human health. Researchers are also testing new cancer treatments in dogs with the hope that these therapies could help people.

Giving an experimental drug to healthy dogs is different from treating sick dogs. Bannasch says Loyal’s drug will need to clear a high safety bar for owners to be comfortable giving it to their pets. She also thinks a drug would need to show more than a few months of life extension before people would want to buy it for their dogs. “As a pet owner, I think anything over a year would be great. I suspect people would be really interested in that,” she says.

Linda Rhodes says that humans owe it to dogs to make up for the genetic misfortunes they’ve inherited due to hundreds of years of breeding. “We’ve bred dogs to have problems because we want them to look or act a certain way,” she says. “It’s our responsibility to figure out how we can help.”

[snehalblog]

Antibiotic Resistance Market: Key Drivers, Challenges, and Opportunities for Growth - UnivDatos

Antimicrobial resistance (AMR) refers to the ability of a microorganism (bacteria, virus, fungi, parasite) to become resistant to practicable drugs. It is a grave, intricate, and expensive developmental challenge to public health. Statistics established by the Centres for Disease Control and Prevention reveal that each year in America at least 2.8 million antibiotic-resistant infections develop and over 35,000 deaths are caused by the same. AMR is a complex problem that needs an approach in both human and veterinary medicine.

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Recent Developments by the Food & Drug Administration:

· September 25, 2024: The FDA said it will be providing funds for three projects to track, assess, and report data on antimicrobial use in animals. These projects assist in the development of long-term antimicrobial use (AMU) data collection plans being established in the U.S such as proposed Public-Private Partnership Structures External Link Disclaimer for tracking AMU data.

· July 15, 2024: The FDA cleared the Simplexa C. auris Direct developed by DiaSorin Molecular LLC as a molecular-based assay designed to detect Candida auris DNA from a skin swab of the axillary or inguinal area from patients who are suspected to be colonized with C.auris. The test is designed to be useful for the prevention and control of this C. auris infection in health-care facilities. The assay may enable healthcare workers to diagnose patients with colonization by C. auris sooner than traditional turf-based processes when such testing is required. Quicker diagnosis can assist with preventing the transmission of this organism, which is often multi-resistant to azoles including echinocandins, and can contribute to severe illness in immunocompromised hospitalized patients. Such testing is intended to be applied together with other clinical, epidemiologic, and laboratory data that are within the reach of the clinician working on the patient. The test should not be used to diagnose or for regular assessment or treatment of C. auris infection. This is the latest in an ongoing effort by the FDA to ensure that tests for emerging infectious pathogens are developed and expanded.

· June 21, 2024: Sirturo (bedaquiline) switched to traditional approval by the FDA since certain confirmation trials confirmed therapeutic effectiveness. Sirturo is used for the treatment of pulmonary tuberculosis caused by Mycobacterium tuberculosis resistant to at least rifampin and isoniazid; multi-drug-resistant tuberculosis in combination with other agents for adults as well as for pediatrics 5 years old and above, weighing at least 15 kg. Sirturo was the first of its kind to get approval in December 2012 through the FDA’s Accelerated Approval program. During its original designation, the FDA insisted that the applicant had to carry out a confirmatory clinical trial and establish a patient registry on serious adverse events.

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Conclusion:

In conclusion, the healthcare market has recorded a rising trend through the years due to technological enhancements, and growing concern in antibiotic resistance. According to the UnivDatos, increasing cases of antibiotic-resistant infections and increasing investment in antibiotic research & development activities across the globe will drive the scenario of the antibiotic resistance market. As per their “Antibiotic Resistance Market” report, the global market was valued at ~USD 8.3 billion in 2023, growing at a CAGR of about 5.4% during the forecast period from 2024-2032.

[mrunalijadhav]

Veterinary Orthotics-Prosthetics Market Drivers Shaping the Future of Animal Healthcare and Rehabilitation

The veterinary orthotics-prosthetics market has seen significant growth in recent years due to an increasing demand for advanced solutions to enhance the mobility and quality of life for animals. Veterinary orthotics and prosthetics (O&P) refer to devices designed to assist animals suffering from mobility issues caused by injury, disease, or congenital conditions. These devices are typically custom-made to suit the unique anatomical structure of each animal, offering both functional and therapeutic benefits. With the rising awareness about animal healthcare and a greater emphasis on improving animal welfare, several key drivers have emerged, fueling the expansion of this market.

Growing Awareness of Animal Healthcare

One of the most significant drivers of the veterinary orthotics-prosthetics market is the increasing awareness surrounding animal healthcare. As more pet owners recognize the importance of medical treatments and rehabilitation for their animals, the demand for customized orthotic and prosthetic devices has risen. Pets, especially dogs and cats, often experience joint disorders, fractures, or amputations, necessitating rehabilitation through these devices. As people become more conscious of their pets' well-being, they are seeking solutions to manage pain, improve mobility, and ultimately enhance their quality of life.

Advancements in Veterinary Medicine and Technology

Technological advancements in veterinary medicine play a vital role in driving the veterinary orthotics-prosthetics market. The continuous development of 3D printing, CAD (computer-aided design) software, and materials science has led to more precise, effective, and affordable orthotic and prosthetic devices. These innovations have allowed for better customization of devices, ensuring a perfect fit for animals while improving comfort and mobility. In addition, the use of high-tech materials that mimic the natural movement of joints and bones has contributed to more durable and efficient solutions for pets.

Increase in Pet Ownership and Humanization of Pets

The humanization of pets has played a crucial role in the growth of the veterinary orthotics-prosthetics market. As pets are increasingly seen as members of the family, pet owners are willing to invest in treatments that enhance their pets' health and overall well-being. The rising number of pet adoptions, particularly in urban areas, has created a growing market for specialized healthcare solutions. With an increasing focus on providing pets with the same quality of care as humans, the demand for advanced orthopedic treatments and mobility devices has surged.

Rising Incidence of Pet Injuries and Disabilities

The rising incidence of injuries, diseases, and disabilities in pets has further contributed to the growth of the veterinary orthotics-prosthetics market. Accidents, joint issues, and congenital abnormalities have become more prevalent in both domestic and wild animals, necessitating the use of specialized orthotics and prosthetics. Dogs, for example, are particularly prone to hip dysplasia, fractures, and ligament tears, leading to the increasing demand for joint braces, prosthetic limbs, and other mobility aids. The aging population of pets also requires more frequent interventions to manage conditions like arthritis, driving the need for orthopedic solutions.

Support from Veterinary Professionals and Research

Veterinary professionals and research institutions play a crucial role in the development and adoption of orthotic and prosthetic devices. As more veterinary professionals embrace these technologies, they are not only improving treatment outcomes but also educating pet owners about the benefits of orthotic and prosthetic solutions. Additionally, ongoing research and clinical trials continue to optimize the design and functionality of these devices. With a growing body of evidence supporting the effectiveness of O&P treatments in animals, the market is expected to continue expanding.

Expanding Veterinary Care Networks and Facilities

The expansion of veterinary care networks and specialized animal hospitals has also contributed to the growth of the veterinary orthotics-prosthetics market. Veterinary clinics that offer specialized services, including orthotics and prosthetics, are becoming more common. This expansion has made these treatments more accessible to pet owners, leading to an increase in demand for customized solutions. As these services become more mainstream, pet owners are more likely to explore O&P devices as viable options for their animals' care.

In conclusion, the veterinary orthotics-prosthetics market is driven by a combination of factors, including increasing awareness of animal healthcare, technological advancements, the humanization of pets, rising pet injuries, and support from veterinary professionals. These drivers are shaping the future of veterinary care and rehabilitation, ultimately improving the lives of countless animals around the world.

[anujmrfr]

Veterinary CRO and CDMO Market Size, Growth Outlook 2035

The Veterinary CRO and CDMO Market Size was estimated at 6.82(USD Billion) in 2023. The Veterinary CRO and CDMO Market Industry is expected to grow from 7.34(USD Billion) in 2024 to 13.80(USD Billion) by 2032. The Veterinary CRO and CDMO Market CAGR (growth rate) is expected to be around 8.20% during the forecast period (2024 - 2032)

Market Overview The Veterinary CRO and CDMO Market is witnessing significant growth due to the increasing demand for contract research organizations (CROs) and contract development and manufacturing organizations (CDMOs) in the animal health industry. These organizations provide outsourcing solutions for pharmaceutical development, clinical trials, regulatory affairs, and manufacturing of veterinary medicines and vaccines. With the rising prevalence of zoonotic diseases, increasing pet ownership, and growing investment in animal health R&D, the demand for veterinary contract research and manufacturing services is escalating.

Market Size and Share The Veterinary CRO and CDMO Market Size was estimated at 6.82(USD Billion) in 2023. The Veterinary CRO and CDMO Market Industry is expected to grow from 7.34(USD Billion) in 2024 to 13.80(USD Billion) by 2032. The Veterinary CRO and CDMO Market CAGR (growth rate) is expected to be around 8.20% during the forecast period (2024 - 2032). North America dominates the market due to the presence of leading veterinary pharmaceutical companies, stringent regulations, and increased spending on pet healthcare. Europe follows closely, while the Asia-Pacific veterinary contract research market is growing rapidly due to expanding livestock industries and increasing demand for animal vaccines and therapeutics.

Market Drivers

Rising Investment in Animal Health Research: Increased funding for veterinary drug development is boosting market growth.

Growing Pet Ownership and Livestock Population: The rising demand for companion animal pharmaceuticals and livestock vaccines is fueling the need for veterinary contract development services.

Regulatory Complexity Driving Outsourcing: Strict regulatory requirements for veterinary drugs have led to increased reliance on veterinary regulatory affairs outsourcing.

Cost-Effectiveness of Outsourcing Services: Veterinary pharmaceutical companies are turning to CROs and CDMOs to reduce operational costs and accelerate drug development timelines.

Challenges and Restraints

High Cost of Veterinary Clinical Trials: Conducting animal health clinical trials can be expensive, impacting smaller firms.

Regulatory Hurdles and Compliance Issues: Strict global regulations for veterinary pharmaceuticals and biologics can slow market growth.

Limited Availability of Skilled Professionals: The lack of trained personnel for veterinary contract manufacturing and research services is a challenge.

Market Trends

Increasing Focus on Biologics and Veterinary Vaccines: Companies are expanding their veterinary biologics manufacturing capabilities to meet the rising demand.

Adoption of Digital Technologies in Veterinary Research: The integration of AI and big data analytics in veterinary clinical trials is improving efficiency.

Strategic Collaborations and Acquisitions: Companies are engaging in mergers and acquisitions to strengthen their animal health contract services portfolio.

Regional Analysis

North America: Leading market due to well-established animal health CROs and CDMOs, stringent regulatory frameworks, and high veterinary healthcare spending.

Europe: Growing demand for veterinary contract services in pharmaceutical and vaccine production.

Asia-Pacific: Fastest-growing region, driven by increasing livestock production, rising awareness about animal disease prevention, and growing investments in veterinary healthcare.

Rest of the World: Moderate market growth, with potential expansion in Latin America and the Middle East.

Segmental Analysis

By Service Type:

Veterinary Contract Research Services

Veterinary Contract Development & Manufacturing Services

Regulatory Affairs & Consulting Services

By Animal Type:

Companion Animals (Dogs, Cats, Horses, etc.)

Livestock Animals (Cattle, Poultry, Swine, etc.)

By End-User:

Veterinary Pharmaceutical Companies

Biotechnology Firms

Animal Research Institutes

Key Market Players

Charles River Laboratories

IQVIA

InVentiv Health

Thermo Fisher Scientific

Eurofins Scientific

Catalent

Recent Developments

Expansion of Veterinary CDMO Capabilities: Companies like Zoetis and Boehringer Ingelheim are increasing their contract manufacturing capacities for veterinary biologics.

Launch of AI-Based Veterinary Research Platforms: Advanced AI-driven veterinary clinical trial solutions are improving research accuracy.

Strategic Mergers and Acquisitions: Key players are acquiring smaller veterinary CROs to strengthen market presence.

For more information, please visit us at marketresearchfuture

[global-research-report]

Veterinary CRO and CDMO Market Size, Share, and Competitive Landscape

The global veterinary CRO and CDMO market size is expected to reach USD 11.42 billion by 2030, registering a CAGR of 8.94% over the forecast period, according to a new report by Grand View Research, Inc. The market is driven by several factors, including the growing number of expert contract research & manufacturing organizations in developing countries, rising adoption of outsourcing services in key stages of veterinary product developments, increasing animal healthcare investments by major players, and growing demand for novel therapeutic products. In addition, the rising adoption of companion animals and growing demand for animal-derived food products are increasing the need for the mass production of medicines.

Therefore, employing the network of third-party Contract Development & Manufacturing Organizations (CDMO) and Contract Research Organizations (CRO) favors the production scale on time with reduced financial risk. The COVID-19 pandemic caused the market downturn, especially during the year 2020. The primary challenges experienced by the majority of contract outsourcing organizations were enormous resource allocation shifts from non-covid to covid medicines (targeting human applications), supply shortages of veterinary raw materials & APIs, transportation & logistics disruption, and the need for more transparency with the vendors. In addition, other difficulties, such as establishing interruption-free, timely, and reliable supply chains, have added more complexity to outsourcing organizations in developing or manufacturing veterinary products.

However, the market growth quickly recovered the following year with significant measures implemented by key players and contract organizations. While it created numerous challenges, the pandemic also set new trends, such as increased ownership rates of companion animals and pet humanization, coupled with improved animal care expenditure and widened R&D activities in the context of global awareness of prognostic and diagnostic measures. According to the American Pet Products Association, pet care expenditure in the U.S. increased from USD 90.5 billion in 2018 to 123.6 billion in 2021. These factors are anticipated to support the employment of contract research, development, and manufacturing organizations by key players in the long run.

Veterinary CRO And CDMO Market Report Highlights

The key players in the animal health industry are adopting contract outsourcing over in-house manufacturing processes owing to the comprehensive services offered by CROs and CDMOs with extensive capabilities, such as highly reliable resources and technical expertise

The livestock animal segment dominated the industry in 2022 owing to the large production rate of vaccines, pharmaceuticals, and infectious disease diagnostic products specifically for food-producing animals. The companion animal segment is expected to grow at the fastest CAGR during the projected period

The development segment generated the largest revenue share of the animal health CRO & CDMO market in 2022. Whereas, the discovery segment is anticipated to register the fastest CAGR during the forecast period

The medicine segment led the industry in 2022. New outbreaks of infectious diseases are increasing the need for veterinary R&D activities with significant expenditure on novel drug launches. Therefore, CROs are contributing largely to the smooth discovery and development processes

North America was the leading region in 2022 due to the strong presence of key players coupled with the increased number of drug development and veterinary product launch activities in the region

Key companies are implementing significant measures and strategies to enhance their industry presence. For instance, in October 2022, Klifovet (a part of Argenta Group), a combined CRO and CDMO dedicated to animal health, acquired Ondax Scientific to expand its footprint in Western and Southern Europe

Veterinary CRO And CDMO Market Segmentation

Grand View Research has segmented the global veterinary CRO and CDMO market based on animal type, service type, application, and region:

Veterinary CRO And CDMO Animal Type Outlook (Revenue, USD Million, 2018 - 2030)

Companion Animals

Livestock Animals

Veterinary CRO And CDMO Service Type Outlook (Revenue, USD Million, 2018 - 2030)

Discovery

Development

Early Phase/Preclinical

Late Phase/Clinical

Manufacturing

Packaging & Labeling

Market Approval & Post-marketing

Veterinary CRO And CDMO Application Outlook (Revenue, USD Million, 2018 - 2030)

Medicines

Pharmaceuticals

Biologics

Others

Medical Devices

Veterinary CRO And CDMO Regional Outlook (Revenue, USD Million, 2018 - 2030)

North America

US

Canada

Europe

UK

Germany

France

Italy

Spain

Rest of Europe

Asia Pacific

China

Japan

India

Australia

South Korea

Rest of APAC

Latin America

Brazil

Mexico

Rest of LATAM

Middle East & Africa

South Africa

Saudi Arabia

Rest of MEA

Key Players of Veterinary CRO And CDMO Market

Labcorp Drug Development

Charles River Laboratories

clinvet

KLIFOVET GmbH (Argenta Group)

OCR – Oncovet Clinical Research

knoell - Triveritas

Veterinary Research Management

VETSPIN

IDEXX Laboratories

Zoetis – Nexvet

Vetio

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[researchyblog]

Poultry Antibiotic Market Size, Trends, and Growth Forecast to 2025

The global poultry antibiotic market is projected to experience steady growth, driven by the increasing demand for poultry products and the need to manage poultry diseases effectively.

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Market Overview:

Market Size and Growth: The global poultry antibiotic market was valued at approximately USD 2.0 billion in 2023 and is expected to grow at a compound annual growth rate (CAGR) of 6% from 2023 to 2030, reaching an estimated USD 3.0 billion by 2030.

Market Drivers: Key factors contributing to market growth include the rising global population, leading to increased demand for protein sources like poultry; the prevalence of various poultry diseases necessitating effective antibiotic treatments; and heightened animal health concerns prompting the use of antibiotics to maintain poultry health.

Key Market Insights:

Product Segmentation: The market is categorized based on antibiotic types, including penicillins, tetracyclines, macrolides, lincosamides, and aminoglycosides. Each class serves specific therapeutic purposes in poultry health management.

Mode of Administration: Antibiotics are administered through various methods such as oral, injection, and other routes, depending on the specific requirements of the poultry and the nature of the disease being treated.

Distribution Channels: Distribution occurs through veterinary pharmacies, online channels, and other outlets, ensuring accessibility to poultry farmers and veterinary professionals.

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Regional Analysis:

North America: The region holds a significant share of the poultry antibiotic market, driven by advanced poultry farming practices and a high demand for poultry products.

Europe: Europe also represents a substantial market share, with stringent regulations influencing the use of antibiotics in poultry farming.

Asia-Pacific: The Asia-Pacific region is anticipated to witness notable growth due to increasing poultry consumption and the expansion of poultry farming in countries like China and India.

Challenges:

The poultry antibiotic market faces challenges such as the development of antibiotic-resistant bacteria, leading to stricter regulations on antibiotic use; consumer concerns regarding antibiotic residues in poultry products; and the need for sustainable and alternative disease management practices to reduce reliance on antibiotics.

Recent Developments:

There is a growing emphasis on reducing antibiotic usage in poultry farming to combat antibiotic resistance. This shift has led to increased mortality rates in poultry, highlighting the need for balanced approaches that protect animal welfare and public health.

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https://rollbol.com/blogs/1836497/Veterinary-Therapeutics-Market-Share-Overview-Competitive-Analysis-and-Forecast-2031

The Veterinary Therapeutics Market in 2023 is US$ 49.7 billion, and is expected to reach US$ 79.34 billion by 2031 at a CAGR of 6%.

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Veterinary Oncology Market Size, Share And Trends Analysis Report

The global veterinary oncology market size is expected to reach USD 3.11 billion in 2030 and is projected to grow at a CAGR of 12.08% from 2025 to 2030. Increasing prevalence of cancer in pets and demand for veterinary diagnostics are projected to drive the market over the forecast period.

Adoption of canine cancer registry globally to estimate cancer incidences is another driving factor for the market growth. According to frontiers in Veterinary Science in February 2019, the Swiss Canine Cancer Registry (SCCR) was used as a data source and was compiled for future comparative studies of canine and human cancers. This database is further helpful in mitigating the incidence of malignant tumors in the human population, thereby driving the market growth.

Researchers carrying out studies focused on veterinary oncology are further boosting the veterinary oncology market growth. For instance, University of Illinois in August 2017, carried out study that involves more precise detection of metastasis (spread of cancer through the body) for head and neck tumors in dogs. Moreover, the market players are also focusing on new product innovation and strategic collaborations. For instance, in 2018 AdvaVet, a subsidiary of Oasmia Pharmaceutical AB, developed XR17 technology, which is nanoparticle formulation based that makes a single Active Pharmaceutical Ingredient (API) or multiple APIs water soluble. It is a combination therapy and is also a standard treatment for a number of cancer diseases in pet animals. 

Gather more insights about the market drivers, restrains and growth of the Veterinary Oncology Market

Veterinary Oncology Market Report Highlights

• Increasing prevalence of cancer in companion animals, several clinical trial studies to evaluate the safety and effectiveness of cancer therapeutics for pets and technological advancements in veterinary oncology treatment are anticipated to create growth opportunities in the market.

• Chemotherapy accounted for the largest revenue share over the coming years, owing to its increasing adoption for pet cancer treatment either alone or in combination with other therapies.

• The canine segment held the largest revenue share of over 86.09% in 2024, increasing the population of dogs and high prevalence of cancer in dogs as compared to cats.

• North America held the dominant share as of 2024, due to the favorable government policies, new product launch by the companies, and huge investment for veterinary oncology treatment.

• Asia Pacific is anticipated to witness lucrative growth due to increasing focus on animal health and expenditure, increasing number of pet population being exposed to cancer, government focus on animal safety, and several initiatives to curb cancer cases in pet animals.

Veterinary Oncology Market Segmentation

Grand View Research has segmented the global Veterinary Oncology market report based on product, type of waste, end use, and region:

Veterinary Oncology Animal Type Outlook (Revenue, USD Million, 2018 - 2030)

• Canine

• Feline

• Equine

Veterinary Oncology Therapy Outlook (Revenue, USD Million, 2018 - 2030)

• Radiotherapy 

o Stereotactic Radiation Therapy

o LINAC

o Other Types

o Conventional Radiation Therapy

o Surgery

o Chemotherapy

o Immunotherapy

o Other Therapies

Veterinary Oncology Cancer Type Outlook (Revenue, USD Million, 2018 - 2030)

• Skin Cancers

• Lymphomas

• Sarcomas

• Others

Veterinary Oncology Regional Outlook (Revenue, USD Million, 2018 - 2030)

• North America

o U.S.

o Canada

o Mexico

• Europe

o UK

o Germany

o France

o Italy

o Spain

o Denmark

o Sweden

o Norway

o Rest of EU

• Asia Pacific

o Japan

o China

o India

o Australia

o South Korea

o Thailand

o Rest of APAC

• Latin America

o Brazil

o Argentina

o Rest of LA

• Middle East and Africa

o South Africa

o Saudi Arabia

o UAE

o Kuwait

o Rest of MEA

Order a free sample PDF of the Veterinary Oncology Market Intelligence Study, published by Grand View Research.

[lovelypol]

Phenobarbital Market: Climbing to $2.1 Billion by 2033 💊📈

Phenobarbital Market involves the production, distribution, and utilization of phenobarbital, a barbiturate widely used for its anticonvulsant properties in the treatment of epilepsy and as a sedative. This market includes pharmaceutical manufacturers, healthcare providers, and distribution channels ensuring access to this essential medication. The market’s growth is fueled by the rising prevalence of neurological disorders, regulatory approvals, and advancements in drug formulations, leading to improved treatment outcomes and expanding therapeutic applications.

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In 2023, the phenobarbital market was valued at 300 million units, with projections indicating it will rise to 450 million units by 2033. The pharmaceuticals sector, particularly the anti-seizure medication segment, leads the market, driven by the increasing prevalence of epilepsy. The veterinary medicine sub-segment also plays a crucial role, as phenobarbital is widely used for canine epilepsy treatment. The injectable form dominates, with a 55% market share, followed by oral formulations (30%) and rectal formulations (15%). The injectable segment’s popularity is due to its rapid onset of action, essential for emergency therapeutic interventions.

Geographically, North America holds the largest share of the market, bolstered by advanced healthcare infrastructure and a high incidence of epilepsy. Europe follows closely, driven by a strong pharmaceutical sector and supportive healthcare policies. Within countries, the United States leads in market performance, supported by significant R&D investments and a large patient population. Germany ranks second, benefiting from a strong manufacturing base and growing awareness of neurological disorders.

Key players in the market include Pfizer Inc., Sanofi, and Hikma Pharmaceuticals, with Pfizer leading due to its broad distribution network and innovative product offerings. Competitive dynamics are shaped by regulatory frameworks like FDA and EMA guidelines, as well as ongoing R&D efforts for improved formulations and delivery systems.

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[gis56]

Phenobarbital Market: $1.2B → $2.1B by 2033 📈 (5.7% CAGR)

Phenobarbital market is witnessing significant growth, driven by its essential applications in epilepsy, sedation, and seizure management. This barbiturate continues to be a cornerstone in treating neurological disorders, benefiting both human and veterinary medicine.

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In 2023, the market reported a robust volume of 300 million units, projected to surge to 450 million by 2033, reflecting a 10% annual growth rate. Injectable phenobarbital dominates with a 55% market share due to its rapid onset, essential in emergency care. Oral formulations follow at 30%, favored for long-term management.

North America leads the charge, fueled by advanced healthcare systems and a high epilepsy prevalence. The United States stands out with substantial R&D investments and innovative treatment approaches. Europe secures the second spot, with Germany and the UK driving demand through strong pharmaceutical manufacturing and supportive healthcare policies.

Asia-Pacific emerges as a growth hub, with expanding healthcare infrastructure in China and India. Latin America and the Middle East & Africa present moderate opportunities, with Brazil and South Africa showing gradual adoption of advanced treatments.

Key players like Pfizer Inc., Sanofi, and Hikma Pharmaceuticals dominate the competitive landscape. Investments in R&D for novel formulations and delivery systems are shaping the market’s future. However, regulatory hurdles and rising generic competition require strategic agility.

As demand for effective epilepsy and neurological disorder treatments grows, the Phenobarbital market is poised for sustained expansion, offering improved therapeutic outcomes and innovative healthcare solutions.

#PhenobarbitalMarket #EpilepsyTreatment #HealthcareInnovation #NeurologicalDisorders #SeizureManagement #PharmaTrends #BarbiturateDrugs #R&DInvestment #GlobalHealthcare #PharmaceuticalIndustry #AsiaPacificGrowth #HealthcareInfrastructure #DrugFormulations #EmergencyCareSolutions #InnovativeHealthcare