Associated tags: CO, Elective surgery, Surgeon, Injury, Patient, Pharmaceutical, Biotechnology, Therapy, Nerve, Health, Physician, Neurology, Pharmaceutical industry, Research, FDA, Wallerian degeneration, Nerve injury, Science, EVP, Pfizer, Axon, Other Health, General Health, Clinical Trials
Locations: PENNSYLVANIA, UNITED STATES, NORTH AMERICA, AURORA, PHILADELPHIA, PA
Retrieved on:
Thursday, February 22, 2024
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Lead author At the 24-week mark, NTX-001 continues to demonstrate an encouraging safety profile, with lower treatment-emergent adverse event rates than the standard of care.
Key Points:
- At the 24-week mark, NTX-001 continues to demonstrate an encouraging safety profile, with lower treatment-emergent adverse event rates than the standard of care.
- The secondary endpoints, including the Numerical Pain Rating Scale, also showed statistically significant improvements, favoring NTX-001 at the 24-week timepoint.
- Neuraptive Therapeutics, Inc. is dedicated to the innovation and development of medical products and therapeutics to repair and regenerate peripheral nerves.
- Neuraptive Therapeutics, Inc. disclaims any obligation to update the information contained in these forward-looking statements.
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Pharmaceutical industry Neuraptive Therapeutics Inc., a leader in innovative medical solutions, is pleased to announce that it has received Orphan Drug Designation from the United States (US) Food and Drug Administration (FDA) for its fusogen contained in the NTX-001 treatment kit.
Key Points:
- Neuraptive Therapeutics Inc., a leader in innovative medical solutions, is pleased to announce that it has received Orphan Drug Designation from the United States (US) Food and Drug Administration (FDA) for its fusogen contained in the NTX-001 treatment kit.
- Dr. Seth Schulman, Chief Medical Officer of Neuraptive Therapeutics Inc., stated, “Receiving the Orphan Drug Designation for NTX-001 is a testament to our commitment to advancing healthcare solutions for patients impacted by peripheral nerve injuries who today have limited options.” The Orphan Drug Designation is granted to drugs intended to treat rare diseases or conditions in the US.
- Highlights of Orphan Designation are:
Eligibility to receive regulatory assistance and guidance from the FDA in the design of an overall drug development plan.
- “ Following this designation, Neuraptive Therapeutics plans to accelerate the development of NTX-001, aiming to bring this promising treatment to patients as soon as possible.” Said Mr. Tzanis.
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SOC,
EVP Neuraptive Therapeutics, Inc. is dedicated to revolutionizing patient care through innovative therapies, and NTX-001 has the potential to redefine the standard of care.
Key Points:
- Neuraptive Therapeutics, Inc. is dedicated to revolutionizing patient care through innovative therapies, and NTX-001 has the potential to redefine the standard of care.
- Key highlights from the NEUROFUSE Study:
The NEUROFUSE Study is a 48-week, Multicenter, Randomized, Controlled, Evaluator-Blinded Study comparing NTX-001 as an adjunct treatment to standard of care vs. standard of care alone.
- The study was to enroll 60 patients, and patients were randomized in a 1:1 ratio between treatments.
- For more information about Neuraptive Therapeutics, Inc., and our pioneering work in peripheral nerve injury treatments, please visit Neuraptive.com.
Retrieved on:
Monday, February 27, 2023
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Pharmaceutical industry to the company’s Board of Directors.
Key Points:
- to the company’s Board of Directors.
- “On behalf of the Neuraptive Board and its directors, we are excited to welcome Cary to the board,” said Robert Radie, chairman, and chief executive officer of Neuraptive.
- “Cary’s extensive background in the capital markets, corporate strategy, legal, and compliance make him an important addition to the Neuraptive board of directors.
- Mr. Sucoff has been a member of the Bar of the State of New York (now retired) since 1978.
Retrieved on:
Thursday, November 17, 2022
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Research Key Points:
- View the full release here: https://www.businesswire.com/news/home/20221117005443/en/
On behalf of the Neuraptive Board and its directors, we are excited to welcome Bob to the board, said Robert Radie, chairman, and chief executive officer of Neuraptive.
- His extensive experience in drug research and development is a great addition to the Neuraptive board at this important time.
- Dr. Ruffolo is the retired President of Research and Development of Wyeth Pharmaceuticals, and Corporate Senior Vice President of the Wyeth Corporation (now Pfizer).
- Prior to Wyeth, Dr. Ruffolo held executive roles at SmithKline Beecham Pharmaceuticals (now GlaxoSmithKline) and Lilly Research Laboratories.
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Research Neuraptive Therapeutics, Inc., a biotechnology company dedicated to developing novel therapeutics and medical products to address the unmet needs of physicians and patients impacted by peripheral nerve injuries, announced key organizational and financial updates.
Key Points:
- Neuraptive Therapeutics, Inc., a biotechnology company dedicated to developing novel therapeutics and medical products to address the unmet needs of physicians and patients impacted by peripheral nerve injuries, announced key organizational and financial updates.
- Evan Tzanis has been appointed to the role of Chief Operating Officer and Executive Vice President of Research and Development.
- Additionally, Mr. Tzanis has played an integral role guiding the company through significant organizational transition and fundraising.
- Neuraptive Therapeutics, Inc. is a biotechnology company dedicated to developing novel therapeutics and medical products to address the unmet needs of physicians and patients impacted by peripheral nerve injuries.
