Ultra-thinly traded nano cap Trevi Therapeutics (TRVI +56.8%) is up on double normal volume, a scant 16K shares, on the heels of its Q4 report that included an update on its two lead indications.
The Phase 2b/3 PRISM study
evaluating nalbuphine ER in prurigo nodularis patients with severe
pruritus (itchy skin) is ~45% enrolled. Once the 50% threshold is
breached, expected next quarter, a sample size re-estimation analysis
for the primary endpoint will be conducted about mid-year.
Enrollment is underway in a Phase 2 clinical trial, CANAL,
evaluating nalbuphine ER for the treatment of chronic cough in up to 56
patients with ideopathic pulmonary fibrosis. Topline data should be
available in H2.
Nalbuphine ER is an orally administered
extended-release formulation of nalbuphine, a mixed ĸ-opioid receptor
agonist and µ-opioid receptor antagonist that has been approved and
marketed as an injectable for pain indications for more than 20 years
in the United States and Europe. Nalbuphine is the only opioid approved
in the U.S. (and most of Europe) that is not classified as a controlled
substance since it blocks µ-opioid receptors which are responsible for
the euphoric effects of opioids. K-opioid receptors play a key role in
itching, coughing and certain movement disorders.
https://seekingalpha.com/news/3552169-trevi-therapeutics-up-57-on-advancement-of-key-programs
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