🇺🇸 FDA
Pipeline program

GR1014 Cutaneous Gel, The placebo ingredients are identical to those of GR1014-CG with the exception that the drug substance (amifostine) and hydrochloric acid (used at the hydrolysis step to convert amifostine in the active substance, amifostine thiol) are omitted.

GRA.05.SPR.0001

Phase 2 small_molecule active

Quick answer

GR1014 Cutaneous Gel, The placebo ingredients are identical to those of GR1014-CG with the exception that the drug substance (amifostine) and hydrochloric acid (used at the hydrolysis step to convert amifostine in the active substance, amifostine thiol) are omitted. for Radiation-induced dermatitis (radiodermatitis) is a Phase 2 program (small_molecule) at Pharma Mar S.A. with 1 ClinicalTrials.gov record(s).

Program details

Company
Pharma Mar S.A.
Indication
Radiation-induced dermatitis (radiodermatitis)
Phase
Phase 2
Modality
small_molecule
Status
active

Clinical trials