BBI-940 + Fulvestrant for Breast Cancer
(KOMODO-1 Trial)
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial tests a new treatment called BBI-940 for individuals with advanced breast cancer. Researchers are studying BBI-940 alone or with fulvestrant (a hormone therapy) to assess its safety and effectiveness. The trial seeks participants with specific types of breast cancer, such as estrogen receptor-positive or triple-negative with certain characteristics. Participants should have previously tried standard treatments but still require other options. As a Phase 1 trial, the research focuses on understanding how the treatment works in people, offering participants the opportunity to be among the first to receive this new treatment.
Do I have to stop taking my current medications for the trial?
The trial protocol mentions a 'washout period' (time without taking certain medications) for recent anticancer therapy, but it doesn't specify about other medications. It's best to discuss your current medications with the trial team to get specific guidance.
Is there any evidence suggesting that this trial's treatments are likely to be safe?
Previous studies have shown that Fulvestrant is a safe and well-tolerated treatment for advanced breast cancer that is hormone-receptor-positive and HER2-negative. Some patients experienced side effects like nausea and diarrhea, but serious side effects were uncommon.
BBI-940 remains in the early stages of testing, so complete safety information is not yet available. As this is the first human trial for BBI-940, the primary goal is to assess its safety. Early lab tests suggest it targets cancer cells effectively, but researchers are closely monitoring for any side effects in people.
Overall, Fulvestrant has an established safety record, while researchers are studying BBI-940 to understand its safety in humans.12345Why are researchers excited about this trial's treatments?
Researchers are excited about BBI-940 because it offers a fresh approach to treating ER+/HER2- breast cancer, especially in cases without an ESR1 mutation, where the standard treatments usually involve hormone therapies like tamoxifen or aromatase inhibitors. BBI-940 works by targeting specific pathways that are not typically addressed by existing hormone therapies, potentially offering a new line of defense against cancer cells. Additionally, BBI-940 is taken orally, making it a more convenient option compared to some existing treatments that require intravenous administration. This novel mechanism and delivery method could mean fewer side effects and greater convenience for patients.
What evidence suggests that this trial's treatments could be effective for breast cancer?
Research has shown that BBI-940 targets specific proteins called kinesins, which assist cancer cells in dividing and growing. This treatment aims to reduce cancer cell survival by eliminating extra DNA that often promotes cancer growth. Early studies have shown promising results, with BBI-940 reducing cancer cell numbers in breast cancer models. In this trial, some participants will receive BBI-940 combined with fulvestrant, which blocks estrogen—a hormone many breast cancers require for growth. This combination aims to enhance effectiveness by attacking the cancer in multiple ways. Other participants will receive BBI-940 alone, either in dose escalation or at the recommended dose for expansion, to further evaluate its effectiveness.12356
Who Is on the Research Team?
Robert C. Doebele, MD, PhD
Principal Investigator
Boundless Bio, Inc.
Are You a Good Fit for This Trial?
This trial is for adults with advanced or metastatic breast cancer, including certain hormone receptor types. Participants must have already tried standard treatments, be able to swallow pills, and have good organ function. Tumor tissue samples are needed for testing.Inclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Dose Escalation
Participants receive BBI-940 monotherapy in multiple sequential dose escalation cohorts to evaluate safety and determine the recommended dose for expansion (RDE).
Dose Expansion
Participants receive BBI-940 at the recommended dose for expansion (RDE) in defined participant populations, including combination with fulvestrant for specific cohorts.
Follow-up
Participants are monitored for safety and effectiveness after treatment, including assessment of treatment emergent adverse events and progression-free survival.
What Are the Treatments Tested in This Trial?
Interventions
- BBI-940
- Fulvestrant
Trial Overview
The study tests a new oral drug called BBI-940 alone or combined with fulvestrant in people with advanced breast cancer. It’s an early-phase (Phase 1), open-label trial to find the best dose and check safety.
How Is the Trial Designed?
4
Treatment groups
Experimental Treatment
Participants receive BBI-940 given alone in multiple sequential dose escalation cohorts. BBI-940 is given orally in repeated 28-day cycles.
Participants receive BBI-940 given alone at the recommended dose for expansion (RDE). BBI-940 is given orally in repeated 28-day cycles.
Participants receive BBI-940 given alone at the recommended dose for expansion (RDE). BBI-940 is given orally in repeated 28-day cycles.
Participants receive BBI-940 in combination with fulvestrant. BBI-940 is given orally in repeated 28-day cycles at one of multiple potential dose levels.
Find a Clinic Near You
Who Is Running the Clinical Trial?
Boundless Bio
Lead Sponsor
Boundless Bio, Inc.
Lead Sponsor
Citations
1.
investors.boundlessbio.com
investors.boundlessbio.com/news-releases/news-release-details/boundless-bio-presents-preclinical-breast-cancer-data-its-oral/Boundless Bio Presents Preclinical Breast Cancer Data ...
... 940 supports our recently initiated, first-in-human KOMODO-1 clinical trial evaluating BBI-940 in ER+/HER2- and TNBC-LAR breast cancer patients.
Study of the Kinesin Oral Molecular Degrader BBI-940 in ...
Part 2B evaluates BBI-940 monotherapy at the RDE in participants with ER+/HER2- breast cancer with FGFR1 amplification. Part 2C evaluates BBI-940 monotherapy at ...
3.
trial.medpath.com
trial.medpath.com/clinical-trial/e73292fe8467e8ae/nct07408089-BBI-940-first-human-advanced-metastatic-breast-cancerStudy of the Kinesin Oral Molecular... | Clinical Trial - MedPath
Part 2B evaluates BBI-940 monotherapy at the RDE in participants with ER+/HER2- breast cancer with FGFR1 amplification. Part 2C evaluates BBI- ...
4.
stocktitan.net
stocktitan.net/news/BOLD/boundless-bio-presents-preclinical-breast-cancer-data-from-its-oral-lim86q7sw1sc.htmlBoundless Bio details BBI-940 breast cancer data
Data showed ecDNA depletion and reduced cancer cell viability, supporting the ongoing Phase 1 KOMODO-1 trial in advanced or metastatic ...
Boundless Bio Advances BBI-940 in First-in-Human Trial
Trial Progress**: Boundless Bio is advancing its KOMODO-1 clinical trial for BBI-940 targeting ER+/HER2- breast cancer patients, with initial
6.
investors.boundlessbio.com
investors.boundlessbio.com/static-files/6ec7a5f4-6055-4569-aacb-3e09042f05afUnlocking a New Paradigm in Cancer Treatment via ...
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