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Clinical Trials/NCT06435455
NCT06435455
Not yet recruiting
Phase 1

A Phase Ib/II Clinical Study Evaluating the Safety, Tolerability, Pharmacokinetics and Efficacy of GH21 Capsule Combined With D-1553 Tablets in Patients With Locally Advanced or Metastatic Solid Tumors Harboring KRAS G12C Mutation

Suzhou Genhouse Bio Co., Ltd.0 sites126 target enrollmentJuly 1, 2024

Overview

Phase
Phase 1
Intervention
GH21
Conditions
Locally Advanced or Metastatic Solid Tumors Harboring KRAS G12C Mutation
Sponsor
Suzhou Genhouse Bio Co., Ltd.
Enrollment
126
Primary Endpoint
Dose-limiting Toxicities Incidence Count Among Study
Status
Not yet recruiting
Last Updated
last year

Overview

Brief Summary

This s a multi-center, open-label phase Ib/II study to evaluate the safety, tolerability, pharmacokinetics, and efficacy of GH21 combined with D-1553 in patients with advanced or metastatic solid tumors harboring KRAS G12C mutation.

Detailed Description

This study includes 2 parts: dose escalation(Phase Ib) and dose expansion (Phase II). The objective of the dose escalation part is to evaluate the safety, tolerability and pharmacokinetics of GH21 in combination with D-1553 in patients with advanced solid tumors harboring KRAS G12C mutation and to determine the RP2D for the combination therapy. In the dose expansion part, preliminary efficacy and safety of the combination therapy at the RP2D will be further explored in patients with specific cancer harboring KRAS G12C mutation.

Registry
clinicaltrials.gov
Start Date
July 1, 2024
End Date
December 31, 2027
Last Updated
last year
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Suzhou Genhouse Bio Co., Ltd.
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • The patient or his legal representative is able to understand and voluntarily sign a written informed consent (before commencing this study and any research procedure);
  • Age ≥18 years old, male or female;
  • KRAS G12C mutant advanced solid tumor;
  • ECOG Performance Status of 0 or 1
  • At least one measurable lesion as defined by RECIST 1.1

Exclusion Criteria

  • acute myocardial infarction, unstable angina pectoris, coronary artery bypass grafting, cerebrovascular accident, or transient ischemic attack within 6 months before first administration; Grade III-IV heart failure based on the New York Heart Association Cardiac Function Scale at screening; During screening, echocardiography (ECHO) showed left ventricular ejection fraction (LVEF) ≤50%;
  • Patients who have a history of severe allergy, or have a history of allergy to the experimental drug/any excipient/combination drug, or have a history of allergy to multiple drugs;
  • There is an active infection (≥ grade 2) requiring anti-infective treatment or an unexplained fever exceeding 38 ° C within 28 days before the first dose;
  • Any toxicity from previous antitumor therapy prior to initial administration has not returned to CTCAE 5.0 rating ≤ Class 1 (unless hair loss, grade 2 peripheral neuropathy, and/or other grade ≤2 adverse events that do not pose a safety risk);
  • Pregnant and lactating women;
  • The investigator considers that there are any clinical or laboratory abnormalities or other reasons to be unsuitable for participating in this clinical study.

Arms & Interventions

"GH21 + D-1553" Group

GH21 capsules combined with D-1553 tablets were administrated orally

Intervention: GH21

"GH21 + D-1553" Group

GH21 capsules combined with D-1553 tablets were administrated orally

Intervention: D-1553

Outcomes

Primary Outcomes

Dose-limiting Toxicities Incidence Count Among Study

Time Frame: 2 years

Incidence of dose limiting toxicities (DLTs) in the dose escalation phase.

Participants Number of Participants Reporting Adverse Events (AEs) or Serious Adverse Events (SAEs)Objective

Time Frame: 2 years

All patients participating in this study will be assessed for incidence and severity of adverse events (AEs) and serious AEs, including changes in laboratory values, vital signs , etc

Secondary Outcomes

  • response rate (ORR) based on RECIST 1.1 criteria(2 years)
  • Disease Control Rate (DCR) based on RECIST 1.1 criteria(2 years)
  • Progression-free survival (PFS) based on RECIST 1.1 criteria(2 years)
  • Overall survival (OS)(2 years)
  • Area under the plasma concentration-time curve (AUC)(2 years)
  • Duration of response (DOR) based on RECIST 1.1 criteria(2 years)
  • Plasma concentration (Cmax)(2 years)
  • Time to achieve Cmax (Tmax)(2 years)

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