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CTX-009 for Colon Cancer (COMPANION-003 Trial)
Phase 2
Waitlist Available
Research Sponsored by Compass Therapeutics
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up from c1d1 to death from any cause, average of 9 months
Awards & highlights
No Placebo-Only Group
Summary
This trial is testing a new treatment called CTX-009 in patients whose colorectal cancer has spread. The goal is to see if it can shrink the tumors or stop them from growing.
Who is the study for?
Adults over 18 with metastatic colorectal cancer that's been previously treated with specific chemotherapy regimens. They must have measurable cancer lesions, adequate liver and kidney function, and no severe heart or blood pressure issues. Women of childbearing potential and men must agree to use effective contraception.
What is being tested?
The trial is testing CTX-009 in patients with advanced colorectal cancer using an open-label, adaptive two-stage design. Stage one will enroll about 37 patients; if successful, stage two will add another 47 patients to assess the drug's effectiveness.
What are the potential side effects?
While not explicitly listed here, common side effects for cancer treatments like CTX-009 may include nausea, fatigue, increased risk of infection due to lowered immunity, possible liver or kidney function changes, and reactions at the infusion site.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ from c1d1 to death from any cause, average of 9 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~from c1d1 to death from any cause, average of 9 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Overall Response Rate
Secondary study objectives
Disease Control Rate
Duration of Response
Exposure Response by Pharmacokinetic (PK) Sampling
+4 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: CTX-009 TreatmentExperimental Treatment1 Intervention
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for colorectal cancer include chemotherapy, targeted therapy, and immunotherapy. Chemotherapy agents like oxaliplatin and irinotecan work by damaging the DNA of cancer cells, preventing them from dividing and growing.
Targeted therapies, such as cetuximab and bevacizumab, inhibit specific molecules involved in cancer cell growth and blood vessel formation, respectively. Understanding these mechanisms helps patients and doctors choose the most effective treatment plan, manage side effects, and improve overall outcomes by tailoring therapy to the cancer's specific characteristics.
A Multidisciplinary Approach for the Personalised Non-Operative Management of Elderly and Frail Rectal Cancer Patients Unable to Undergo TME Surgery.Resection of hepatic metastases from colorectal cancer. Biologic perspective.
A Multidisciplinary Approach for the Personalised Non-Operative Management of Elderly and Frail Rectal Cancer Patients Unable to Undergo TME Surgery.Resection of hepatic metastases from colorectal cancer. Biologic perspective.
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Who is running the clinical trial?
Compass TherapeuticsLead Sponsor
4 Previous Clinical Trials
397 Total Patients Enrolled
Thomas J Schuetz, MD, PhDStudy DirectorCompass Therapeutics
Minori Rosales, MD, PhDStudy DirectorCompass Therapeutics
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Eligibility Criteria:
This trial includes the following eligibility criteria:- I had chemotherapy or targeted therapy for colorectal cancer less than 4 weeks ago.I am a woman who can have children and have a negative pregnancy test.I have brain metastases that are causing symptoms or are not under control.I am 18 years old or older.My primary tumor was removed over 3 months ago.My cancer has worsened after 2 or 3 treatments for advanced stages.I have received all approved targeted therapies for my tumor's specific mutations.I have had heart problems in the last 5 years.I had radiation therapy less than 2 weeks ago.I do not have a severe infection needing strong antibiotics or have any uncontrolled infectious diseases.My liver and kidney functions are within normal ranges.I can carry out all my usual activities without help.I am following the required birth control guidelines.My colorectal cancer has spread or come back.I haven't taken certain medications recently.I had surgery or a major procedure less than 4 weeks ago.I haven't had cancer immunotherapy or experimental drugs in the last 4 weeks.My left-sided tumor is RAS wild type and I've had anti-EGFR therapy.I have a history of bleeding or stomach-related diseases.My previous treatments included specific chemotherapy drugs.
Research Study Groups:
This trial has the following groups:- Group 1: CTX-009 Treatment
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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