Active, not recruitingPHASE1, PHASE2NCT04349436

Study to Investigate the Efficacy and Safety of RP1 in Adult Patients With Organ Transplants and Advanced Skin Malignancies

Studying Cutaneous neuroendocrine carcinoma

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Key facts

Sponsor
Replimune Inc.
Principal Investigator
Jeannie Hou, MD
Replimune Inc.
Intervention
RP1, intra-tumoral injection, oncolytic virus(biological)
Enrollment
69 enrolled
Eligibility
18 years · All sexes
Timeline
20202029

Study locations (28)

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT04349436 on ClinicalTrials.gov

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