New Triple-Action antibody takes on Hard-to-Treat cancers
NCT ID NCT06598800
First seen Jun 24, 2026 · Last updated Sep 11, 2026 · Updated 3 times
Summary
This early-phase study tests a new drug called BG-T187, a special antibody that targets two proteins (EGFR and MET) on cancer cells. It is given alone or with other drugs to people with advanced solid tumors that have spread or cannot be removed. The main goals are to check safety, find the right dose, and see if the drug can shrink tumors. About 153 participants will take part in this first-in-human trial.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- BG-T187 (a trispecific antibody targeting EGFR and MET proteins)
- What this could lead to
- If successful, this could lead to a new treatment option for people with advanced solid tumors that have not responded to other therapies.
- What could go wrong
- This is an early phase 1 trial with only 153 participants, so the drug may not be safe or effective. Side effects could be serious, and the drug may not shrink tumors.
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.
- Phase
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Phase 1
The first testing in people. Mainly checks safety and dose, usually in a small group.
- Participants
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About 153 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Oct 2024
- Expected to finish
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Sep 2028
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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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 Hide 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: 1. Able to provide a signed and dated written informed consent prior to any study-specific procedures, sampling, or data collection. 2. Participants must be ≥ 18 years of age or the legal age of consent in the jurisdiction in which the study is taking place. 3. Eastern Cooperative Oncology Group (ECOG) Performance Status ≤ 1. 4. Participants with selected histologically or cytologically confirmed advanced, metastatic, and unresectable solid tumors who have been previously treated, including but not limited to non-small cell lung cancer (NSCLC), colorectal cancer (CRC). 5. ≥ 1 measurable or nonmeasurable lesion as assessed by RECIST v1.1. for Phase 1a Part A; ≥ 1 measurable lesion per RECIST v1.1. for Phase 1a Part B and Phase 1b. 6. Adequate organ function. Exclusion Criteria: 1. Prior severe allergic reactions or hypersensitivity to the active ingredient and excipients of BG-T187 or other monoclonal antibodies. 2. Spinal cord compression, active leptomeningeal disease, or uncontrolled, untreated brain metastasis. 3. Any malignancy ≤ 3 years before the first dose of study drug(s) except for the specific cancer under investigation in this study and any locally recurring cancer that has been treated with curative intent (eg, resected basal or squamous cell skin cancer, superficial bladder cancer, or carcinoma in situ of the cervix or breast). 4. History of interstitial lung disease (ILD) or noninfectious pneumonitis requiring steroids or other immune suppressive agents ≤ 2 years before the first dose of the study drug, or with current ILD/noninfectious pneumonitis, or where suspected ILD/noninfectious pneumonitis cannot be ruled out by imaging during screening. 5. Uncontrollable pleural effusion, pericardial effusion, or ascites requiring frequent drainage (recurrence ≤14 days after intervention). 6. Active hepatitis C. 7. Infection (including tuberculosis infection, or other) requiring systemic (oral or intravenous) antibacterial, antifungal, or antiviral therapy ≤ 14 days before the first dose of study drug(s). Note: Other protocol defined Inclusion/Exclusion criteria may apply.
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Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The study's own enquiry address
This study publishes an address for enquiries. See it below .
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The places running it
34 sites in 4 countries. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Show contact details
Enter your email to view the contact information for this study.
Genom att skicka in godkänner du våra Användarvillkor
Study contacts
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Contact
Email: •••••@•••••
Locations
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Affiliated Zhongshan Hospital of Fudan University
RECRUITINGShanghai, Shanghai Municipality, 200032, China
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Asan Medical Center
RECRUITINGSongpaGu, Seoul Teugbyeolsi, 05505, South Korea
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Blacktown Cancer and Haematology Centre
RECRUITINGBlacktown, New South Wales, NSW 2148, Australia
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Cabrini Hospital Malvern
RECRUITINGMalvern, Victoria, VIC 3144, Australia
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Cancer Hospital Chinese Academy of Medical Sciences
RECRUITINGBeijing, Beijing Municipality, 100021, China
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Chongqing University Cancer Hospital
RECRUITINGChongqing, Chongqing Municipality, 400030, China
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Fujian Cancer Hospital
RECRUITINGFuzhou, Fujian, 350014, China
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Fujian Medical University Union Hospitalqishan Branch
RECRUITINGFuzhou, Fujian, 350108, China
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Guangxi Medical University Cancer Hospital
RECRUITINGNanning, Guangxi, 530021, China
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Hackensack University Medical Center
RECRUITINGHackensack, New Jersey, 07601-1915, United States
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Harbin Medical University Cancer Hospital
RECRUITINGHarbin, Heilongjiang, 150000, China
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Hubei Cancer Hospital
RECRUITINGWuhan, Hubei, 430079, China
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Hunan Cancer Hospital
RECRUITINGChangsha, Hunan, 410013, China
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Liaoning Cancer Hospital and Institute
RECRUITINGShenyang, Liaoning, 110042, China
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Linear Clinical Research
RECRUITINGNedlands, Western Australia, WA 6009, Australia
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Linyi Peoples Hospital
RECRUITINGLinyi, Shandong, 276000, China
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Macquarie University
RECRUITINGNorth Ryde, New South Wales, NSW 2109, Australia
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Next Oncology Virginia
RECRUITINGFairfax, Virginia, 22031, United States
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Samsung Medical Center
RECRUITINGGangnamGu, Seoul Teugbyeolsi, 06351, South Korea
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Seoul National University Bundang Hospital
RECRUITINGSeongnam-si, Gyeonggi-do, 13620, South Korea
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Seoul National University Hospital
RECRUITINGSeoul, Seoul Teugbyeolsi, 03080, South Korea
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Severance Hospital Yonsei University Health System
RECRUITINGSeodaemunGu, Seoul Teugbyeolsi, 03722, South Korea
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Shanxi Provincial Cancer Hospital
RECRUITINGTaiyuan, Shanxi, 030013, China
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The Catholic University of Korea, Seoul St Marys Hospital
RECRUITINGSeochoGu, Seoul Teugbyeolsi, 06591, South Korea
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The Catholic University of Korea, St Vincents Hospital
RECRUITINGPaldalGu SuwonSi, Gyeonggi-do, 16247, South Korea
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The First Affiliated Hospital of Nanchang University Branch Xianghu
RECRUITINGNanchang, Jiangxi, 332000, China
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The First Affiliated Hospital, Zhejiang University School of Medicinezhijiang Branch
RECRUITINGHangzhou, Zhejiang, 310024, China
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The Fourth Hospital of Hebei Medical University
RECRUITINGShijiazhuang, Hebei, 050011, China
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The Sixth Affiliated Hospital, Sun Yat Sen University
RECRUITINGGuangzhou, Guangdong, 510655, China
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The University of Texas Md Anderson Cancer Center
RECRUITINGHouston, Texas, 77030-4009, United States
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Tianjin Medical University Cancer Institute and Hospital
RECRUITINGTianjin, Tianjin Municipality, 300060, China
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Tongji Hospital of Tongji Medical College Huazhong University of Science and Technology
RECRUITINGWuhan, Hubei, 430030, China
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Washington University, St Louis, Division of Oncology
RECRUITINGMadison, Wisconsin, 53708-8056, United States
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Zhejiang Cancer Hospital
RECRUITINGHangzhou, Zhejiang, 310022, China
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- First-in-Human trial asks whether HG381 is safe and tolerable in advanced solid tumors
- Custom-Built immune cells take aim at a notorious cancer mutation
- Experimental injection SHR-7787 put to the test against advanced solid tumors
- Experimental biologic AWT020 put to the test in Hard-to-Treat cancers
- Can a pill shrink Hard-to-Treat ovarian tumors?
- Oral drug RVU120 put to the test against advanced solid tumors