Fact CheckerSign in

NCT05009329Active, not recruitingPhase 1/2

A Study of JAB-21822 in Adult Patients With Advanced Solid Tumors Harboring KRAS p.G12C Mutation in China

Multi-center, Open, Dose-escalation, and Expanded Phase I/II Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Antitumor Activity of JAB-21822 in Advanced Solid Tumors With KRAS p.G12C Mutation

Source: ClinicalTrials.gov · Last updated 13 Aug 2026

Brief summary (registry, in English)

To assess safety, tolerability, PK, efficacy and determine recommended phase 2 dose (RP2D) of JAB-21822 (glecirasib) administered in adult participants with KRAS p.G12C-mutant advanced solid tumors.

Status (registry)
Active, not recruiting
Phase (registry)
Phase 1/2
Study type
Interventional
Enrollment
315 (actual)
First submitted
26 Jul 2021
Start date
26 Jul 2021
Primary completion date
Aug 2026
Lead sponsor
Allist Pharmaceuticals, Inc.
Diseases
Lung cancer
NCT number
NCT05009329

What you commit to

  • Study type: Interventional · Phase 1/2
  • Participants enrolled: 315
  • From 26 Jul 2021 to the primary completion date, Aug 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previously treated with KRAS G12C inhibitor
  • Previous allogeneic bone marrow transplant or organ transplant
  • Intended study subjects who were unable to abstain from alcohol during medication

Other illness

  • History of intestinal disease or major gastric surgery or inability to swallow oral medications
  • Other active cancer
  • Active infection including hepatitis B, hepatitis C and human immunodeficiency virus (HIV)
  • Impaired heart function or clinically significant heart disease
  • Other unqualified conditions judged by the investigators

Other

  • Pregnant or breast-feeding

Who the study is looking for

  • Written informed consent
  • Advanced (metastatic or unresectable) KRAS p.G12C mutant solid tumors, with failure or absence of standard treatment
  • Subject must be ≥18 years
  • Eastern Cooperative Oncology Group (ECOG) Performance Status score of 0 or 1.
  • Subjects with life expectancy ≥3 months.
  • Subjects must have at least one measurable lesion as defined by RECIST v1.1.
  • There was no serious organ dysfunction in the screening stage
  • Male or female subjects of reproductive age agree to use adequate contraception

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Beijing Cancer Hospital
Coordinator of this site? Confirm its status
BeijingChinaUnknown status

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.