Brief: Helix Biopharma accelerates escalation of L-DOS47 dosing in the U.S. Phase I study
Nov 30 (Reuters) - Helix Biopharma Corp HBP.TO
* Helix Biopharma Corp accelerates escalation of L-DOS47
dosing in the U.S. Phase I study
* Helix Biopharma - U.S. FDA has accepted accelerated
escalation for L-DOS47 dosing in U.S. Phase I study up to
12g/kg in combination with pemetrexed/carboplatin
Source text for Eikon: ID:nCCN7HBZRx
Further company coverage: HBP.TO
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