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NCT07030257 · Tasca Therapeutics

Study of CP-383 in Patients With Advanced or Metastatic Solid Tumors

What this study is about

The goal of this clinical trial is to learn if an experimental drug CP-383 works to treat advanced cancer. It will also learn about the safety of CP-383.

View original scientific description

The goal of this clinical trial is to learn if an investigational drug CP-383 works to treat advanced cancer. It will also learn about the safety of CP-383. The main questions if aims to answer are: * Does CP-383 slow or stop the growth of cancer in patients with advanced cancer * What medical problems do participants have when taking CP-383 Researchers will test CP-383 in all kinds of cancers at various dose levels to determine what the best dose is to study further.

Interventions

DRUG

CP-383

Novel anti-cancer agent inhibiting pyrimidine synthesis in cancer cells

Primary outcome measures

Part 1: Determine the maximum tolerated dose (MTD)

Time frame: 21 days

Determine the MTD of CP-383 in subjects with advanced solid tumors

Part 2: Evaluate the efficacy of CP-383 at the recommended phase 2 dose in selected tumor types

Time frame: From enrollment through study completion, an average of 1 year

Objective response rate assessed by the investigator according to RECIST

Who can participate

This study lists these criteria on ClinicalTrials.gov. A study coordinator reviews eligibility during screening — this page does not determine whether you qualify.

Inclusion criteria

  • Measurable or non measurable cancer that the research can assess for changes
  • Not eligible or able to take existing standard therapies for cancer
  • Availability of a part of a tumor for laboratory testing or willing to have a safe biopsy taken from a tumor
  • Diagnosed with locally advanced, recurrent or metastatic incurable disease
  • Part 1: any solid tumor (with the exception of brain cancer) that has progressed, standard therapy is no longer or has not helped the cancer, or is too toxic and for whom a clinical trial is an option for continued treatment
  • Part 1: specific advanced, metastatic tumor types will also be enrolled: colorectal cancer, small cell lung cancer, head and neck cancer, non-small cell lung cancer, pancreatic cancer, bladder cancer - some of these will have a specific gene mutation in the cancer
  • Part 1: selected solid tumor cancer types (with the exception of brain cancers) that have a specific gene mutation in the cancer
  • Part 2: specifi

Where

  • Denver, Colorado
  • Orlando, Florida
  • Grand Rapids, Michigan
  • St Louis, Missouri
  • Omaha, Nebraska
  • Huntersville, North Carolina
  • Cleveland, Ohio
  • Maumee, Ohio
  • Philadelphia, Pennsylvania
  • Dallas, Texas
  • San Antonio, Texas
  • West Valley City, Utah

And 1 more location — see the full list below.

Related conditions & keywords

Solid Tumor MalignanciesColorectal CarcinomaSmall Cell Lung Cancer ( SCLC )Head and Neck (HNSCC)Bladder CancerNon-Small Cell Lung CancerPancreatic Cancer, Advanced or MetastaticPhase 1Dose EscalationDose ExpansionLoss of FunctionFAT1P300

Frequently asked questions

What is a clinical trial?

A clinical trial is a research study that tests new medical treatments, drugs, devices, or procedures to determine their safety and effectiveness. Trials are carefully designed and monitored to protect participants while advancing medical knowledge.

Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. Trials must be reviewed and approved, and participants are closely monitored by medical professionals throughout the study. You can withdraw at any time if you choose.

Will I be compensated?

Many clinical trials offer compensation for your time, travel expenses, and inconvenience. The specific compensation varies by study and will be discussed during the screening process. All study-related medical care is typically provided at no cost to participants.

Will I receive a placebo instead of treatment?

When effective treatment exists, participants typically receive either the standard treatment plus the study intervention, or the standard treatment plus placebo. You would not be denied effective care. Placebos are primarily used when no proven treatment is available, or in addition to standard care. Your trial consent form will clearly explain what treatments you may receive.

Can I leave a trial if I change my mind?

Absolutely. Participation in clinical trials is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty or loss of benefits to which you are otherwise entitled.

How long does a clinical trial last?

Trial duration varies widely depending on the study design and purpose. Some trials last just a few weeks, while others may continue for months or years. The study coordinator will provide specific timeline information during your screening call.

Data: ClinicalTrials.gov · synced Feb 18, 2026 · Source of record for eligibility and locations

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1 of 150 participants interested
1% interest

See if this study fits

A short prescreen based on this study's listed criteria. A coordinator confirms eligibility — this is not a medical assessment.

Preparing your pre-screening questions…

Study locations

Choose your preferred location, or select flexible during enrollment.

RECRUITING

Denver

Colorado

Location available
RECRUITING

Orlando

Florida

Location available
RECRUITING

Grand Rapids

Michigan

Location available
RECRUITING

St Louis

Missouri

Location available
RECRUITING

Omaha

Nebraska

Location available
View Omaha location page
RECRUITING

Huntersville

North Carolina

Location available
RECRUITING

Cleveland

Ohio

Location available
RECRUITING

Maumee

Ohio

Location available
RECRUITING

Philadelphia

Pennsylvania

Location available

And 4 more locations available.

Express your interest

Share your contact details and a study coordinator can follow up about screening.

Secure & Confidential

Your information is protected and will only be shared with the research team.

What participation can include

  • Study-related care provided by the research team
  • Close monitoring by medical professionals
  • Possible compensation for time and travel*
  • The option to withdraw at any time
  • Contributing to medical research that may help future patients

*Compensation varies by study. Confirm details with coordinator.

Typical next steps

  1. 1.Submit this form
  2. 2.Phone screening
  3. 3.In-person assessment if eligible
  4. 4.Begin participation

Find More Advanced Solid Tumors Trials by City

Browse all advanced solid tumors clinical trials in these cities — not just this study.

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Looking for Solid Tumors Treatment in Denver?

Join others in Colorado exploring innovative treatment options through clinical research

Solid Tumors Treatment Options in Denver, Colorado

If you're searching for Solid Tumors treatment in Denver, participating in a clinical research study may provide access to innovative approaches under expert medical supervision. This study is actively recruiting participants in Denver, Orlando, Grand Rapids and surrounding areas.

Clinical trials offer participants the opportunity to receive cutting-edge treatments while contributing to medical research that may help future patients with Solid Tumors. All study-related care is provided at no cost to participants.

Local Sites
3 locations in Colorado
Now Enrolling
Up to 150 participants
Quick Start
Screening available now

Why Consider a Clinical Trial for Solid Tumors?

Potential Benefits

  • Access to new treatment approaches before public availability
  • Close monitoring by experienced medical professionals
  • Study-related care provided at no cost
  • Contribute to medical research for Solid Tumors

What to Expect

  • Initial screening to determine eligibility
  • Regular check-ups and monitoring visits
  • Possible compensation for time and travel
  • You can withdraw at any time

Frequently Asked Questions About This Solid Tumors Study

Important Clinical Trial Information

This information is provided for educational purposes and does not constitute medical advice. Clinical trial participation involves potential risks and benefits. Eligibility requirements apply and will be assessed during the screening process.

Study identifier: NCT07030257. For complete study details, visit ClinicalTrials.gov. Always consult with your healthcare provider before making decisions about your medical care or participating in clinical research.