Potentia Pharmaceuticals, a privately held biotechnology company, has reported positive Phase I data from the ASaP clinical trial for the company's lead drug candidate, POT-4, which is being developed for the treatment of age-related macular degeneration.
Subscribe to our email newsletter
The ASaP trial is a first-in-man, multi-center, single escalating dose study. The interim results of this trial revealed no drug-related toxicity based on clinical signs, ophthalmic examinations, or laboratory results at any time point monitored in patients treated with up to 150mcg/dose of POT-4. Additionally, no serious adverse events and no identifiable intraocular inflammation were reported.
Preliminary results indicate that intravitreal POT-4 is safe, and the data accumulated so far support the continued investigation of POT-4 for the treatment of both dry and wet age-related macular degeneration (AMD) with larger randomized clinical trials to further define its efficacy profile, the company said.
Cedric Francois, president and CEO of Potentia Pharmaceuticals, said: “These safety data strongly support the further development of POT-4 as a potential treatment for patients with AMD. We believe that the product has significant promise based on these early-stage findings and look forward to further testing of the compound in higher doses as we continue this trial.”
Advertise With UsAdvertise on our extensive network of industry websites and newsletters.
Get the PBR newsletterSign up to our free email to get all the latest PBR
news.