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ACTIVE NOT RECRUITING Phase 1

A Study to Learn About the Study Medicine PF-07985045 When Given Alone or With Other Anti-cancer Therapies in People With Advanced Solid Tumors That Have a Change in a Gene.

NCT06704724 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to learn about the safety and effects of the study medicine when given alone or together with other anti-cancer therapies. Anti-cancer therapy is a type of treatment to stop the growth of cancer. This study also aims to find the best amount of study medication. This study is seeking participants who have solid tumors (a mass of abnormal cells that forms a lump or growth in the body) that: * are advanced (cancer that doesn't disappear or stay away with treatment) and * have a KRAS gene mutation (a change in the DNA of the KRAS gene that can cause cells to grow in very high numbers). This includes (but limited to) the following cancer types: * Non-Small Cell Lung Cancer (NSCLC): It's a type of lung cancer where the cells grow slowly but often spread to other parts of the body. * Colorectal Cancer (CRC): This is a disease where cells in the colon (a part of large intestine) or rectum grow out of control. * Pancreatic ductal adenocarcinoma (PDAC): This is a cancer that starts in the ducts of the pancreas but can spread quickly to other parts of the body. Pancreas is a long, flat gland that lies in the abdomen behind the stomach. Pancreas creates enzymes that help with digestion. It also makes hormones that can help control your blood sugar levels. All participants in this study will take the study medication (PF-07985045) as pill by mouth. This will be repeated for 21-day or 28-day cycles. Depending on which part of the study participants are enrolled into they will receive the study medication (PF-07985045 alone or in combination with other anti-cancer medications). These anti-cancer medications will be given in the study clinic by intravenous (IV) that is directly injected into the veins at different times (depending on the treatment) during the 21-day or 28-day cycle. Participants can continue to take the study medication (PF-07985045) and the combination anti-cancer therapy until their cancer is no longer responding. The study w

Interventions

  • COMBINATION_PRODUCT Gemcitabine
  • COMBINATION_PRODUCT Nab-paclitaxel
  • COMBINATION_PRODUCT Cetuximab
  • COMBINATION_PRODUCT Fluorouracil
  • DRUG PF-07985045

Study Locations (13)

Arkansas

  • Highlands Oncology Group — Fayetteville
  • Highlands Oncology Group — Rogers
  • Highlands Oncology Group — Springdale

Massachusetts

  • Brigham and Women's Hospital — Boston
  • Dana-Farber Cancer Institute — Boston
  • DFCI Chestnut Hill — Newton

New York

  • Columbia University Irving Medical Center — New York
  • The Trustees of Columbia University and The New York and Presbyterian Hospital — New York

Wisconsin

  • University of Wisconsin Carbone Cancer Center - Eastpark Medical Center — Madison
  • University of Wisconsin Carbone Cancer Center-University Hospital — Madison

California

  • City of Hope (City of Hope National Medical Center, City Of Hope Medical Center) — Duarte

Texas

  • The University of Texas MD Anderson Cancer Center — Houston

Other

  • Pan American Center for Oncology Trials, LLC — Rio Piedras

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2024-12-10
Est. Completion 2029-03-11
Phase Phase 1

Sponsor

Pfizer

769 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06704724

The ClinicalTrials.gov registry entry for NCT06704724 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 30 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Pfizer, which has 769 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 Carcinoma, Non-Small-Cell Lung appearing as the primary indexed condition, and to 5 interventions — of which Gemcitabine 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: NCT06704724 reports 13 study locations spanning 7 distinct geographic areas — top geographies include Arkansas, Massachusetts, New York. 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 NCT06704724 about?

NCT06704724 is a clinical study titled "A Study to Learn About the Study Medicine PF-07985045 When Given Alone or With Other Anti-cancer Therapies in People With Advanced Solid Tumors That Have a Change in a Gene.". The purpose of this study is to learn about the safety and effects of the study medicine when given alone or together with other anti-cancer therapies. Anti-cancer therapy is a type of treatment to stop the growth of cancer. This study also aims to find the best amount of study medication. This st...

What is the current status of trial NCT06704724?

This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 30 participants. The study started on 2024-12-10. Estimated completion is 2029-03-11.

What conditions does trial NCT06704724 study?

This clinical trial studies the following conditions: Carcinoma, Non-Small-Cell Lung, Colorectal Neoplasms, Carcinoma, Pancreatic Ductal. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06704724?

The interventions under investigation include: Gemcitabine (COMBINATION_PRODUCT), Nab-paclitaxel (COMBINATION_PRODUCT), Cetuximab (COMBINATION_PRODUCT), Fluorouracil (COMBINATION_PRODUCT), PF-07985045 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06704724?

This trial is sponsored by Pfizer, which has 769 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06704724 being conducted?

This trial has 13 study locations across Arkansas, California, Massachusetts, New York, Texas. 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