Canada's Orcrist Bio, a biotechnology company developing stem cell-mobilizing pharmaceuticals, has filed a Phase I, open-label, single-ascending-dose, safety study of HYC750, treatment for chemotherapy-related blood cell depletion, in healthy male volunteers with the European Competent Authority.
The goal of the study is to assess the safety, tolerability, pharmacokinetics and pharmacodynamics of HYC750, a patent-protected formulation of hyaluronan. Orcrist utilized the regulatory expertise and experience of Netherlands-based Kinesis Pharma to develop the clinical trial submission.
This article is accessible to registered users, to continue reading please register for free. A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.
Login to your accountTry before you buy
7 day trial access
Become a subscriber
Or £77 per month
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed
Chairman, Sanofi Aventis UK
| Headless Content Management with Blaze