Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

ACTIVE NOT RECRUITING Phase 1

A Study to Evaluate the Safety, Pharmacokinetics, and Activity of GDC-6036 Alone or in Combination in Participants With Advanced or Metastatic Solid Tumors With a KRAS G12C Mutation

NCT04449874 · View on ClinicalTrials.gov ↗

Study Summary

This is a Phase I dose-escalation and dose-expansion study that will evaluate the safety, pharmacokinetics (PK), and preliminary activity of GDC-6036 in patients with advanced or metastatic solid tumors with a KRAS G12C mutation.

Interventions

  • DRUG Bevacizumab
  • DRUG Atezolizumab
  • DRUG Cetuximab
  • DRUG Erlotinib
  • DRUG GDC-6036

Study Locations (20)

California

  • City of Hope Comprehensive Cancer Center — Duarte
  • UCSD Moores Cancer Center — La Jolla
  • Chao Family Comprehensive Cancer Center UCI — Orange

Other

  • UZ Antwerpen — Edegem
  • CHU de Liège — Liège
  • AZ St Maarten Campus Leopoldstr — Mechelen

Pennsylvania

  • Abramson Cancer Center — Philadelphia
  • UPMC - Hillman Cancer Center — Pittsburgh

New South Wales

  • St Vincent's Hospital Sydney — Darlinghurst
  • Slade Health Inward goods — Mount Kuring-Gai

Victoria

  • Peter MacCallum Cancer Center — Melbourne
  • Alfred Health — Melbourne

Connecticut

  • Yale Cancer Center — New Haven

Massachusetts

  • Dana Farber Cancer Institute — Boston

Oklahoma

  • University of Oklahoma — Oklahoma City

Trial Details

FieldValue
Enrollment Target 498 participants
Start Date 2020-07-29
Est. Completion 2027-12-31
Phase Phase 1

Sponsor

Genentech

206 total trials

Interested in This Trial?

Always speak with your doctor before enrolling in a clinical trial.

Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT04449874

The ClinicalTrials.gov registry entry for NCT04449874 describes a study currently listed as active not recruiting. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 498 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Genentech, which has 206 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 3 conditions, with Colorectal Cancer appearing as the primary indexed condition, and to 5 interventions — of which Bevacizumab is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT04449874 reports 20 study locations spanning 13 distinct geographic areas — top geographies include California, Other, Pennsylvania. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT04449874 about?

NCT04449874 is a clinical study titled "A Study to Evaluate the Safety, Pharmacokinetics, and Activity of GDC-6036 Alone or in Combination in Participants With Advanced or Metastatic Solid Tumors With a KRAS G12C Mutation". This is a Phase I dose-escalation and dose-expansion study that will evaluate the safety, pharmacokinetics (PK), and preliminary activity of GDC-6036 in patients with advanced or metastatic solid tumors with a KRAS G12C mutation.

What is the current status of trial NCT04449874?

This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 498 participants. The study started on 2020-07-29. Estimated completion is 2027-12-31.

What conditions does trial NCT04449874 study?

This clinical trial studies the following conditions: Colorectal Cancer, Advanced Solid Tumors, Non-Small Cell Lung Cancer. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT04449874?

The interventions under investigation include: Bevacizumab (DRUG), Atezolizumab (DRUG), Cetuximab (DRUG), Erlotinib (DRUG), GDC-6036 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT04449874?

This trial is sponsored by Genentech, which has 206 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT04449874 being conducted?

This trial has 20 study locations across California, Connecticut, Massachusetts, Oklahoma, Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial