The
Phase 1 study was created to work out safety and most dose of EP-100, such as a
suggested dose for Phase 2 trials. Based upon clinical experience of escalating
dosages in 38 affected individuals within the Phase 1 study and on preclinical
studies revealing synergy of EP-100 along with different chemotherapeutic
elements, Esperance has begun joining of affected individuals within a Phase 2
multi‐center trial for
sufferers along with advanced ovarian melanoma randomized to actually EP‐100 in conjunction with paclitaxel versus paclitaxel
alone.
"Results
coming from the Phase 1 study recommend that LHRH expression is a practicable
target for session, understanding that EP-100 has possible being a targeted,
well-tolerated therapeutic for tumor therapy in places in which many affected
individuals are exhausting of alternatives," said lead investigator Ramesh
K. Ramanathan, MD from the Virginia G. Piper Cancer Center/TGen, (Scottsdale,
AZ). "I look forward to carrying on with progress with this particular
exciting, new drug applicant in a number of later step clinical trials."
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