New cancer drug BGB-24714 tested in early trial for solid tumors
NCT ID NCT05381909
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This early-phase study tested a new drug called BGB-24714, which is designed to help cancer cells die. It was given alone or with chemotherapy to 157 adults with advanced solid tumors that had spread or could not be removed. The main goal was to find a safe dose and see how well people tolerated the treatment. The study was terminated early, so full results may not be available.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- BGB-24714 (a drug that helps cancer cells die), given with or without chemotherapy drugs like paclitaxel, carboplatin, or docetaxel
- What this could lead to
- If it works, this could point toward a new treatment option for people with advanced solid tumors that have not responded to other therapies.
- What could go wrong
- This is a very early phase 1 trial, so the main goal is just to find a safe dose. It is too soon to know if the drug will actually shrink tumors or help patients live longer. The trial was also terminated early, so results may be limited.
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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157 people
The number who actually took part.
- Started
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Jul 2022
- Finished
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Jul 2025
- 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.
Key Eligibility Criteria : 1. Participants must sign a written informed consent form (ICF); and agree to comply with study requirement 2. Phase 1a (Dose Escalation): Part A, A-CN, and B: Participants with histologically or cytologically confirmed unresectable locally advanced or metastatic solid tumor previously treated with standard systemic therapy or for whom treatment is not available or not tolerated Note: Only Chinese participants will be eligible for Part A-CN. Part C: Participant has histologically or cytologically confirmed, locally advanced, unresectable Stage III Non-small cell lung cancer (NSCLC) suitable for definitive chemoradiotherapy (CRT) Part D: Participant with locally advanced, histologically confirmed inoperable esophageal squamous cell carcinoma (ESCC) suitable for definitive CRT Phase 1b (Dose Expansion): Participants with histologically or cytologically confirmed solid tumors of selected types previously treated with standard therapy. 3. Participants must be able to provide formalin-fixed paraffin embedded (FFPE) tumor tissue sample. 4. Phase 1a Part A, A-CN, B and Phase 1b: ≥ 1 measurable lesion per Response evaluation criteria in solid tumors (RECIST) v1.1 5. Eastern Cooperative Oncology Group (ECOG) Performance Status ≤ 1 Key Exclusion Criteria: 1. Active leptomeningeal disease or uncontrolled, untreated brain metastasis. 2. 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 3. Any condition that required systemic treatment with either corticosteroids or other immunosuppressive medication ≤ 14 days before the first dose of study drug(s). 4. Clinically significant infection requiring systemic therapy ≤ 14 days before the first dose of study drug(s). 5. Prior exposure to agents with second mitochondria-derived activator of caspases (SMAC) mimetics, or other Inhibitors of apoptosis proteins (IAPs) antagonists. NOTE: Other protocol defined inclusion/exclusion criteria may apply.
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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.
Contacts and locations
Locations
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Asan Medical Center
SongpaGu, Seoul Teugbyeolsi, 05505, South Korea
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Auckland City Hospital
Auckland, 1023, New Zealand
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Austin Health
Heidelberg, Victoria, VIC 3084, Australia
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Avera Cancer Institute
Sioux Falls, South Dakota, 57105-2108, United States
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Banner Md Anderson Cancer Center
Gilbert, Arizona, 85234-2165, United States
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Barbara Ann Karmanos Cancer Institute
Detroit, Michigan, 48201-2013, United States
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Chongqing Cancer Hospital
Chongqing, Chongqing Municipality, 400030, China
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Florida Cancer Specialist (Scri) Sarasota
Sarasota, Florida, 34232, United States
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Gachon University Gil Medical Center
NamdongGu, Incheon Gwang'yeogsi, 21565, South Korea
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Hackensack University Medical Center
Hackensack, New Jersey, 07601-1915, United States
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Henan Cancer Hospital
Zhengzhou, Henan, 450000, China
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Hunan Cancer Hospital
Changsha, Hunan, 410013, China
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Icon Cancer Centre South Brisbane
South Brisbane, Queensland, QLD 4101, Australia
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Intermountain Healthcare
Salt Lake City, Utah, 84143, United States
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Mary Crowley Cancer Research
Dallas, Texas, 75230, United States
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Massachusetts General Hospital
Boston, Massachusetts, 02114, United States
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National Cancer Center (Korea)
IlsandongGu GoyangSi, Gyeonggi-do, 10408, South Korea
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Next Virginia
Fairfax, Virginia, 22031, United States
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Northern Beaches Hospital
Frenchs Forest, New South Wales, NSW 2086, Australia
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Peter Maccallum Cancer Centre
Melbourne, Victoria, VIC 3000, Australia
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Princess Alexandra Hospital
Woolloongabba, Queensland, QLD 4102, Australia
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Samsung Medical Center
GangnamGu, Seoul Teugbyeolsi, 06351, South Korea
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Sanford Cancer Center
Sioux Falls, South Dakota, 57104-4663, United States
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Scri Florida Cancer Specialist East
West Palm Beach, Florida, 33401-3406, United States
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Scri Florida Cancer Specialists North
St. Petersburg, Florida, 33705-1449, United States
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Severance Hospital Yonsei University Health System
SeodaemunGu, Seoul Teugbyeolsi, 03722, South Korea
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Shandong Cancer Hospital
Jinan, Shandong, 250117, China
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Shandong Provincial Hospital
Jinan, Shandong, 250021, China
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Sunshine Hospital
St Albans, Victoria, VIC 3021, Australia
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Tennessee Oncology, Pllc Nashville
Nashville, Tennessee, 37203, United States
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The University of Texas Md Anderson Cancer Center (Department Gi Medical Oncology)
Houston, Texas, 77030-4000, United States
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University of Texas Southwestern Medical Center
Dallas, Texas, 75390-7208, United States
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University of Washington
Seattle, Washington, 98195, United States
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Upmc Hillman Cancer Center(Univ of Pittsburgh)
Pittsburgh, Pennsylvania, 15232-1309, United States
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