Provectus Biopharmaceuticals, Inc. (NYSE MKT:PVCT, http://www.pvct.com), a
development-stage oncology and dermatology biopharmaceutical company
(“Provectus”), announced today that it will be meeting with the U.S. Food and
Drug Administration (the “FDA”) to review certain operational aspects of the
protocol for its planned phase 3 clinical trial of intralesional PV-10, its
novel investigational drug for cancer, as a treatment for melanoma. No date
for this meeting has been agreed upon as yet.
Eric Wachter, PhD, CTO of Provectus, stated, “When we submitted the protocol
to the Agency in November, we included a brief list of questions about certain
operational aspects of the protocol, in particular regarding eligibility
requirements relevant to maximizing the speed of enrollment of patients in the
study. This is standard practice for a pivotal submission. The FDA has
subsequently indicated that a formal meeting is appropriate to assure that
these questions are addressed in a timely and documented manner. We hope the
meeting will occur in January or early February 2015.”
Dr. Wachter added, “We currently have eight sites, four in the U.S. and four
in Australia, in our expanded access program that are using PV-10 for melanoma
and other cutaneous malignancies. They will provide a path to quickly starting
enrollment once this review period is finished. In addition, we expect
additional sites to join the study pending action by their respective
Institutional Review Boards.”
Dr. Wachter concluded, “I want to stress that this meeting with the Agency in
no way affects the fundamental design of the study, and the FDA has given us
no indication that it has any concerns about the proposed study design and
endpoints.”
For a detailed list of the current inclusion and exclusion criteria and
further details regarding the endpoints of the study, visit:
https://clinicaltrials.gov/ct2/show/NCT02288897?term=pv-10&rank=5
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