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Clinical trial

An Open, Dose-exploration Study, Followed by a Randomized, Double-blind, Placebo-controlled Study, to Evaluate the Efficacy and Safety of CVL237 Tablets in Patients With APDS/PASLI

NCT06293716 is registered in ClinicalTrials.gov with Convalife (Shanghai) Co., Ltd. as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
An Open, Dose-exploration Study, Followed by a Randomized, Double-blind, Placebo-controlled Study, to Evaluate the Efficacy and Safety of CVL237 Tablets in Patients With APDS/PASLI
Lead sponsor
Convalife (Shanghai) Co., Ltd.
Phase
Phase 2/3
Overall status
Unknown status
Start date
March 30, 2024
Completion date
March 30, 2026
Enrollment
35 (estimated)
Sites
1

Conditions

As the registry lists them; a condition with its own page is linked.

pi3k and p110delta hyperactivation syndrome