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Blood samples may unlock secrets of cancer drug resistance

NCT ID NCT05272423

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 25, 2026 · Last updated Aug 05, 2026 · Updated 3 times

Summary

This study collects blood samples from up to 500 adults in the US with KRAS G12C-positive cancer whose disease has progressed after treatment with a KRAS inhibitor. Researchers will analyze the samples to identify genetic changes that cause resistance. The goal is to compare resistance patterns between different drugs and cancer types, which may guide future treatment strategies.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

What this could lead to
If successful, this could reveal why some cancers become resistant to KRAS inhibitors, pointing toward better combination treatments.
What could go wrong
This is an observational study, not a treatment trial. It collects data only, so it won't directly help participants. Results may not lead to new therapies quickly.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

58 people

The number who actually took part.

Started

Sep 2022

Finished

Apr 2026

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

Adult subjects with a diagnosis of acquired resistance to KRAS inhibitors

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Cohort 1A- Liquid Biopsy 1. Participants older than 18 years old at the time of consent or age of majority for residential state. 2. Demonstration of having advanced KRAS G12C positive cancer. 3. Systemic progression (not CNS only progression) within the past 30 days, having previously been treated with a therapeutic, targeting the specific KRAS mutation. 4. Patient must not have started a new line of therapy before signing the informed consent form. 5. Willingness to provide a blood specimen prior to the initiation of a new line of treatment. 6. Willingness to provide clinical and medical information to the study team as required. 7. Ability to read, write and communicate in English. 8. Ability to sign a web-based informed consent form. Cohort 1B- Data Sharing 1. Participants older than 18 years old at the time of consent or age of majority for residential state. 2. Demonstration of having advanced KRAS G12C positive cancer. 3. Systemic progression (not CNS only progression) after being treated with a therapeutic targeting the specific KRAS mutation. 4. Patient must have prior tumor genotyping available (tissue or plasma) after progression on therapeutic targeting the specific KRAS mutation. 5. Willingness to provide clinical and medical information to the study team as required. 6. Ability to read, write and communicate in English. 7. Ability of the participant or legally authorized representative (LAR) to sign a web-based informed consent form. Exclusion Criteria: 1. Participants who are unable to comply with the study procedures. 2. Known existence of an uncontrolled intercurrent illness including, but not limited to, psychiatric illness or social situations that would impair compliance with study requirements. 3. Participants who have previously enrolled to the study.

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Dana-Farber Cancer Institute

    Boston, Massachusetts, 02215, United States

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