drugset / Trial / NCT04543344

Study To Evaluate The Pharmacokinetic, Safety And Tolerability Of Single Or Multiple Subcutaneous Doses of Recifercept

NCT04543344 ↗

Phase 1 Completed 24 enrolled Pfizer
RandomizedParallel-groupDouble-blindTreatment

Summary

This will be a single center, randomized, parallel group, repeated dose study of recifercept (Cohort 1 and Cohort 2) or placebo (only in Cohort 1) in approximately 18 healthy participants, using 2 cohorts (N = 9) at two dose levels of recifercept.

Timeline

Start
2020-09-17
Primary completion
2021-08-03
Completion
2021-11-26

Drugs

EvaluationDrugModalityDoseRoute
Subject Recifercept Protein / enzyme biologic — Subcutaneous

Indications

No indication recorded.