WHO ICTRP trial

Study to Evaluate the Safety and Efficacy of Afamelanotide in Patients with…

EUCTR2018-004164-60-NL · EU Clinical Trials Register · Authorised

Key facts

Trial ID EUCTR2018-004164-60-NL
Public title Study to Evaluate the Safety and Efficacy of Afamelanotide in Patients with Variegate Porphyria (VP)-related skin disease
Scientific title A Proof of Concept, Phase IIa, Open Label Study to Evaluate the Safety and Efficacy of Afamelanotide in Patients with Variegate Porphyria (VP)-related skin disease. - Phase IIa VP Study
Primary sponsor CLINUVEL (UK) LTD
Registry EU Clinical Trials Register
Recruitment status Authorised
Study type Interventional clinical trial of medicinal product
Phase Human pharmacology (Phase I): no Therapeutic exploratory (Phase II): yes Therapeutic confirmatory - (Phase III): no Therapeutic use (Phase IV): no
Countries Netherlands;Switzerland
Conditions Variegate Porphyria (VP)-related skin disease;Therapeutic area: Body processes [G] - Metabolic Phenomena [G03]
Interventions Trade Name: SCENESSE Pharmaceutical Form: Implant
Registration date Feb 21, 2022
Target size 6
Secondary IDs CUV040
Registry page clinicaltrialsregister.eu

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