Recruiting
Phase 2

BAY2927088

Sponsor:

Bayer

Code:

NCT06760819

Conditions

Advanced Solid Tumors

HER2 Mutation

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

BAY2927088

Study Details

Brief summary:

Researchers are looking for a better way to treat people who have solid tumors with HER2-activating mutations. Before a treatment can be approved for people to take, researchers do clinical trials to better understand its safety and how it works.

In this trial, the researchers want to learn how well BAY2927088 (sevabertinib) works in people with different types of solid tumors with HER2 mutations. These include tumors in the colon or rectum, the uterus and the cervix (lower part of the uterus), the breast, the bladder, and the biliary tract (includes gall bladder and bile ducts) as well as other types of solid tumors with the exception of people with advanced non-small cell lung cancer (NSCLC).

Solid tumors may have specific changes or mutations to a gene called human epidermal growth receptor-2 (HER2). This leads to the formation of an abnormal form of HER2 protein in the cancer cells, resulting in increased cell growth. The study treatment, BAY2927088, is expected to block the abnormal HER2 protein which may stop the spread of cancer.

The trial will include about 111 participants who are at least 18 years old. All the participants will take 20 mg of BAY2927088 as tablets by mouth.

The participants will take treatments in 3-week periods called cycles. These 3-week cycles will be repeated throughout the trial. The participants can take BAY2927088 until their cancer gets worse, until they have medical problems, or until they leave the trial.

During the trial, the doctors will take imaging scans of different parts of the body to study the spread of cancer and will check heart health using echocardiogram or cardiac magnetic resonance imaging (MRI) and electrocardiogram (ECG). The doctors will also take blood and urine samples and do physical examinations to check the participants' health. They will ask questions about how the participants are feeling and if they have any medical problems.

Conditions

Advanced Solid Tumors

HER2 Mutation

Study ID

NCT06760819

Start date

Feb 13, 2025

Status verified date

Jul 30, 2026

Completion date

Oct 26, 2029

Anticipated

Primary completion date

Feb 2, 2029

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • Documented histologically or cytologically confirmed locally advanced, unresectable or metastatic solid tumor cancer (colorectal carcinoma; biliary tract cancer; bladder and urothelial tract cancer; cervical cancer; endometrial cancer; breast cancer; other solid tumor cancer, excluding NSCLC)
  • Participant must be ≥18 years of age or over the legal age of consent
  • Patients who have received prior standard therapy appropriate for their tumor type and stage of disease, or who have no satisfactory alternative treatments
  • Documented activating HER2 mutation
  • At least one measurable lesion that would qualify as a target lesion by RECIST 1.1 criteria

Exclusion Criteria:

  • Primary diagnosis of non-small cell lung cancer (NSCLC)
  • Prior treatment with a HER2 tyrosine kinase inhibitor (TKI)
  • Active brain metastases
  • Uncontrolled, severe, intercurrent illness

Study Design

Enrollment

111 participants

Anticipated

Allocation

Non randomized

Intervention Model

Single group

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: BAY2927088

Adult participants with metastatic or unresectable solid tumors with HER-2 activating mutations including: colorectal, biliary tract, bladder, cervical, endometrial, breast, and other solid tumor types. Participants will receive BAY2927088 20 mg BID until disease progression per RECICST 1.1, unacceptable toxicity, or until any other withdrawal criteria.

RECIST 1.1 = Response Evaluation Criteria in Solid Tumors, version 1.1; BID: twice a day

Interventions

BAY2927088

tablet, oral

Primary outcome measure

  • Objective Response Rate (ORR) per RECIST 1.1 as assessed by BICR [ Time Frame: From start of study intervention until the first documented progression, or death from any cause, or end of study (up to approximately 3 years), whichever comes first ]

Central Contacts and Locations

Central contacts

Locations

City of Hope - Duarte Cancer Center

Recruiting

Duarte, California, United States, 91010

Florida Cancer Specialists & Research Institute - Fort Myers Cancer Center - Gladiolus

Recruiting

Fort Myers, Florida, United States, 33908

Dana-Farber Cancer Institute - Oncology Department

Recruiting

Boston, Massachusetts, United States, 02215

Cleveland Clinic - Oncology Department

Recruiting

Cleveland, Ohio, United States, 44195

SCRI Oncology Partners

Recruiting

Nashville, Tennessee, United States, 37203

The University of Texas MD Anderson Cancer Center - Texas Medical Center

Recruiting

Houston, Texas, United States, 77030

Princess Margaret Cancer Centre | Medical Oncology and Hematology

Recruiting

Toronto, Ontario, Canada, M5G 2C4

More Information

Sponsor

Bayer

Last update posted

Sep 3, 2026

Last verified

Jul 30, 2026

Keywords

  • Colorectal cancer
  • CRC
  • Biliary tract cancer
  • BTC
  • Bladder cancer
  • Cervical cancer
  • Endometrial cancer
  • Sarcoma
  • Gastrointestinal stromal tumor
  • GIST
  • Breast cancer
  • Gastrointestinal cancer
  • GI cancer
  • Gastric cancer
  • Esophageal cancer
  • Gallbladder cancer
  • Pancreatic cancer
  • Ovarian Cancer
  • Salivary cancer
  • Ampullary cancer
  • Urothelial cancer
  • HER2 mutant cancer

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by Bayer on 2026-09-03.