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Acelarin achieved a disease control rate of 93% in a subset of 14 evaluable patients with advanced gynecological cancers in the PRO-001 study.This was followed by the Phase 1b dose-ranging PRO-002 study where Acelarin in combination with carboplatin achieved a 96% disease control rate and 39% response rate in 23 evaluable patients with recurrent ovarian cancer. 13, 2017 (GLOBE NEWSWIRE) — Apellis Pharmaceuticals, Inc.The primary endpoint of the study will be Objective Response Rate, and secondary endpoints include Duration of Response, Progression-Free Survival, Overall Survival and safety parameters.Part one of the study will enroll up to 20 patients in each of two dose cohorts: 500mg/m2 and 750mg/m2.In part two of the study, Nu Cana will select one of these doses and enroll at least an additional 24 patients at the selected dose.Nu Cana expects to announce interim data from this study in 2018.(NASDAQ: APLS), a clinical-stage biopharmaceutical company focused on the development of novel therapeutic compounds to treat disease through the inhibition of the complement system, today announced the closing of its initial public offering of 10,714,000 shares of common stock at a public offering price of .00 per share.

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SYNB1020 was safe and well tolerated in subjects in multiple ascending dose cohorts who received total daily doses of up to 1.5×1012 CFU for 14 days.

Jitjatjo is a new app specifically designed to solve temporary hospitality staffing problems.

Catering companies, event planners and restaurateurs can use Jitjatjo (which sounds like tic tac toe) to ease their “supply and demand” challenges of staffing.

We are pleased to be a part of this important clinical study.” Acelarin is a potential first-in-class Pro Tide that has been evaluated in over 140 patients.

In the first-in-human Phase 1 dose-ranging PRO-001 study in 49 evaluable patients with advanced metastatic solid tumors, Acelarin was well tolerated and achieved a 78% disease control rate.

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