Cure My Disease

Don't miss your cure!

Home News Browse Soon ready About
Log in / Sign up

Noonan syndrome 3

MONDO:0012371

Any Noonan syndrome in which the cause of the disease is a mutation in the KRAS gene.

Also known as: KRAS Noonan syndrome, KRAS gene related Noonan syndrome, NS3, Noonan syndrome 3, Noonan syndrome caused by mutation in KRAS, Noonan syndrome type 3

15 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Cardiovascular disorder (1051) Disease (680) Heart disorder (300) Musculoskeletal system disorder (207) Hereditary disease (176) Immune system disorder (148) Cardiomyopathy (144) Lymphedema (139) Vascular disorder (135) Hypertrophic cardiomyopathy (112)
Trials to join now! 11 Not yet recruiting 1 Not yet finished but already full! 2 Completed 1
Sort by
  • New combo therapy shows promise for Hard-to-Treat cancers

    Disease control Completed

    This early-phase trial tested a combination of three drugs—vemurafenib, cetuximab, and irinotecan—in 47 people with advanced solid tumors that have a specific BRAF V600 mutation and could not be removed by surgery or had spread. The main goal was to find the safest dose and under…

    Phase: PHASE1 • Sponsor: M.D. Anderson Cancer Center • Aim: Disease control

    Last updated Jun 27, 2026 12:23 UTC

Cure My Disease

Helping patients find clinical trials that match their disease.

Why was Cure my disease built?

Explore

Home News Browse About Terms of use Contact us

This is a site from Cyber and Space