New pill CMS-D017 enters first human safety trials
NCT ID NCT07462780
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This early-stage study tests a new drug called CMS-D017 in 88 healthy adults to see if it is safe and how the body processes it. The drug is being developed for two rare conditions: paroxysmal nocturnal hemoglobinuria (a blood disorder) and complement-mediated kidney disease. Participants will receive either the drug or a placebo, and researchers will monitor side effects and drug levels in the blood.
What this could mean
Our plain-language read of the trial. This is informational only — not medical advice or a prediction.
- Active substance
- CMS-D017 capsule
- What this could lead to
- If safe, this could lead to further studies testing CMS-D017 as a treatment for paroxysmal nocturnal hemoglobinuria and complement-mediated kidney disease.
- What could go wrong
- This is an early Phase 1 trial in healthy people, not patients. It only tests safety and dosing, not whether the drug works for any disease.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for COMPLEMENT-MEDIATED KIDNEY DISEASE are added.
By submitting, you agree to our Terms of use
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Peking University Third Hospital
RECRUITINGBeijing, China
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Could a new pill tame a rare blood disease? early safety trial begins
- New drug pegcetacoplan tested in teens with rare blood disorder
- New PNH drug VSA012 enters early human testing
- Thousands with blood diseases to be tracked in massive chinese registry
- New drug SLN12140 aims to control PNH in early trial
- New siRNA drug ADX-038 enters human trials for PNH anemia