Cision PR Newswire
Fidelis Animal Health, Inc. Announces Major Label Expansion for Ethiqa XR®
Ethiqa XR, an extended-release buprenorphine, adds captive rodents and laboratory rabbits to label for 72-hour control of post-procedural pain.
NORTH BRUNSWICK, N.J., Nov. 5, 2024 /PRNewswire/ -- Fidelis Animal Health, Inc. has received notification from the Food and Drug Administration (FDA) that Ethiqa XR (buprenorphine extended-release injectable suspension) 1.3 mg/mL is now indicated for the control of post-procedural pain in captive rodents and laboratory rabbits. With Ethiqa XR, veterinarians have an FDA-indexed, pharmaceutical grade, cGMP extended-release buprenorphine for use in mice, naked mole rats, gerbils, hamsters, rats, chinchillas, guinea pigs, prairie dogs, ferrets, laboratory rabbits, and non-human primates.
"We are excited to bring these new indications to veterinarians in general and specialty practices, and in the research community. Ethiqa XR meets their high expectations for efficacy, safety, and quality, and makes it so much easier to comply with FDA GFI #256, which stresses the importance of using legal, FDA-indexed animal medications instead of compounded drugs for office stock and individual patient use1," said Michael Wells, Board Chair and CEO.
"Ethiqa XR is an innovative form of buprenorphine that uses Fidelis Animal Health's Fidelipid LAI™ technology, a patented lipid-based formulation that safely delivers 72 hours of clinical analgesia with just one subcutaneous injection2," says Dr. Steven Leary, the company's Chief Medical Officer. "It is manufactured in compliance with cGMP standards, meeting strict specifications to ensure consistency in quality and potency. Ethiqa XR is sterilized, with no harmful excipients, endotoxins, or microbial contamination."
Since its launch to laboratory veterinarians in 2020, Ethiqa XR is currently being used in over five hundred institutions across the country, including those at the top ten pharmaceutical companies, many of the country's elite academic institutions, hospital systems, and several government research facilities. Use is rapidly growing among practicing veterinarians who treat small mammals.
Ethiqa XR is easily and readily available from the major national veterinary distributors, including Covetrus, Patterson, MWI Animal Health and Midwest Veterinary Supply. For more information, visit www.ethiqaxr.com.
IMPORTANT SAFETY INFORMATION
For Captive Rodents, Ferrets, Laboratory Rabbits and Non-Human Primates:
Only administer Ethiqa XR® by subcutaneous injection. Ethiqa XR is not intended for intravenous, intra-arterial, intrathecal, intramuscular, or intra-peritoneal injection. Do not use in animals with pre-existing respiratory compromise.
Death has been reported when non-steroidal anti-inflammatory drugs (NSAIDs such as meloxicam and carprofen) and Ethiqa XR have been administered concomitantly in mice.
Do not house rats on wood chip-type bedding after administration of Ethiqa XR. Pica involving wood chip type bedding can be lethal.
Ethiqa XR may cause sedation, decreased blood pressure, decreased heart rate, decreased gastrointestinal mobility, and respiratory depression. Use caution with concomitant administration of Ethiqa XR with drugs that cause respiratory depression. Animals should be monitored for signs of decreased cardiovascular and respiratory function when receiving Ethiqa XR.
The safety of Ethiqa XR has not been evaluated in pregnant, lactating, neonatal, or immune-compromised animals.
For Humans:
Not for use in humans. Keep out of reach of children and pets.
Ethiqa XR contains buprenorphine, a Schedule III controlled substance with an abuse potential similar to other Schedule III opioids, which may lead to overdose and death.
Ethiqa XR should be handled appropriately to minimize the risk of misuse, abuse, addiction, and criminal diversion, including restriction of access, the use of accounting procedures, and proper disposal methods as appropriate to the laboratory setting and as required by law.
Ethiqa XR should only be handled and administered by a veterinarian, veterinarian technician, or laboratory staff trained in the handling of potent opioids. Wear protective clothing when administering Ethiqa XR to avoid direct contact with human skin, eyes, oral, or other mucus membranes which could result in absorption of buprenorphine and adverse reactions.
For more information, consult the Prescribing Information including the Boxed Warning.
BOXED WARNING | |||
Abuse Potential | |||
Life-Threatening Respiratory Depression | |||
Accidental Exposure | |||
Risks From Concurrent Misuse or Abuse with Benzodiazepines or Other CNS Depressants Concurrent misuse or abuse of opioids with benzodiazepines or other central nervous system (CNS) depressants, including alcohol, may result in profound sedation, respiratory depression, coma, and death. | |||
See HUMAN SAFETY WARNINGS for detailed information.
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About Fidelis Animal Health: Fidelis Animal Health is a commercial stage company offering exceptional expertise in the acquisition, development, and marketing of unique pharmaceutical formulations. The company is committed to leading the industry with developing and bringing to the market quality-driven therapeutics and additional innovations for all animals, small and large, using our proprietary extended- release technology.
For more information about Fidelis Animal Health, please visit www.FidelisAH.com.
Media Inquiries:
Media@FidelisAH.com
- https://www.fda.gov/regulatory-information/search-fda-guidance-documents/cvm-gfi-256-compounding-animal-drugs-bulk-drug-substances; accessed 3/14/2024.
- Ethiqa XR full prescribing information.
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SOURCE Fidelis Animal Health, Inc.
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