FHD-286 + Decitabine + Venetoclax for Acute Myeloid Leukemia
(FHD-286 Trial)
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial explores a new combination of three treatments—Decitabine, Venetoclax, and FHD-286 (an experimental treatment)—to assess their effectiveness in combating acute myeloid leukemia (AML), a type of blood cancer. It targets individuals with AML who have specific risk factors or whose condition has worsened after initial treatment. The study seeks participants diagnosed with AML, especially those facing aggressive or recurring forms of the disease that have not responded to previous treatments. 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 combination therapy.
Do I need to stop my current medications for the trial?
The trial requires stopping certain medications before starting. You must stop strong CYP3A inhibitors at least 1 week before, and strong CYP3A inducers at least 2 weeks before the trial. Proton pump inhibitors must also be stopped or switched 7 days before the trial.
Is there any evidence suggesting that this trial's treatments are likely to be safe?
Research has shown that using Decitabine and Venetoclax together is generally safe for treating patients with acute myeloid leukemia (AML). Studies have found this combination to be effective and safe, particularly for older patients. One study demonstrated improved survival rates and reduced cancer when this treatment was used with other drugs.
An early study on FHD-286 examined its safety at different doses in participants with relapsed or hard-to-treat AML. While specific reports of severe side effects have not emerged, the research aimed to determine a safe dosage.
Overall, research supports the safety of these treatments. However, since this trial is in an early phase, the primary goal is to explore safety and identify the best dose. This phase is crucial for understanding how well participants can tolerate the treatment.12345Why are researchers excited about this trial's treatments?
Researchers are excited about this treatment combination for acute myeloid leukemia (AML) because it introduces FHD-286, a novel compound, alongside established drugs like Decitabine and Venetoclax. FHD-286 is an epigenetic modulator, which means it can potentially alter how genes are expressed in cancer cells, possibly making them more susceptible to treatment. This approach is different from traditional chemotherapy, which targets rapidly dividing cells more broadly. By targeting the cancer cells in a new way, this combination aims to enhance treatment effectiveness and offer new hope for patients with AML.
What evidence suggests that this trial's treatments could be effective for Acute Myeloid Leukemia?
Research has shown that combining Decitabine and Venetoclax significantly improves recovery rates in older patients with Acute Myeloid Leukemia (AML). One study found that this combination nearly doubled the rate of complete recovery compared to other treatments. In this trial, participants will receive a combination of Decitabine, Venetoclax, and FHD-286. FHD-286, a new drug under investigation, targets specific proteins in cancer cells, hindering their survival and growth. Lab studies have shown that when FHD-286 is used with Decitabine and Venetoclax, it reduces cancer and improves survival. These findings suggest this combination could effectively treat AML, especially in challenging cases.13567
Who Is on the Research Team?
Mendel R Goldfinger, MD
Principal Investigator
Montefiore Medical Center
Are You a Good Fit for This Trial?
This trial is for adults with newly diagnosed high-risk acute myeloid leukemia (AML) or AML that has come back after one treatment. Participants must have certain organ function levels, not be on other cancer drugs recently, and cannot join if they’ve already had similar treatments before.Inclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Induction Treatment
Participants receive Decitabine, Venetoclax, and FHD-286 for 12 weeks to reduce tumor burden and improve hematopoiesis
Long-term Treatment
Participants continue treatment as long as they receive clinical benefit, focusing on disease control and hematopoietic improvement
Safety Follow-up
Participants undergo a safety follow-up evaluation 30 days after treatment discontinuation
Long-term Follow-up
Participants are contacted every 2 months to assess survival status and disease progression
What Are the Treatments Tested in This Trial?
Interventions
- Decitabine
- FHD-286
- Venetoclax
Trial Overview
The study tests a combination of three drugs—FHD-286, low-dose decitabine, and venetoclax—in people with difficult-to-treat AML. All participants receive the same treatment to find the safest dose and observe effects.
How Is the Trial Designed?
1
Treatment groups
Experimental Treatment
Administration: * Decitabine is reconstituted with 5 mL of sterile water and given by subcutaneous (SC) injection at the investigational site. * Venetoclax is taken as a tablet provided by the investigational site pharmacy or another authorized specialty pharmacy. * FHD-286 is taken as a capsule provided by the investigational site pharmacy.
Find a Clinic Near You
Who Is Running the Clinical Trial?
Montefiore Medical Center
Lead Sponsor
Foghorn Therapeutics Inc.
Industry Sponsor
Citations
FHD-286 With Low-Dose Weekly Decitabine/Venetoclax in ...
This is a Phase 1, uncontrolled, single-arm, open-label, nonrandomized, dose escalation, study of Decitabine (DAC)+Venetoclax (VEN)+FHD-286 in participants ...
The efficacy and safety of venetoclax combined with ... - PMC
VEN + DEC group (OR 1.90, 95%CI 1.36–2.67) could significantly improve CR among the elderly patients with AML, compared to the control group.
3.
aacrjournals.org
aacrjournals.org/clincancerres/article/31/12/2327/762768/A-Phase-I-Study-of-FHD-286-a-Dual-BRG1-BRM-SMARCA4A Phase I Study of FHD-286, a Dual BRG1/BRM (SMARCA4 ...
This phase I study evaluated the safety of FHD-286 at daily oral doses ranging from 2.5 to 10 mg in 40 patients with relapsed or refractory ...
BRG1/BRM inhibitor targets AML stem cells and exerts ...
Compared with each drug, cotreatment with FHD-286 and BETi, MI, decitabine, or venetoclax significantly reduced AML burden and improved survival ...
Decitabine + Venetoclax Compared with Intensive ...
Superior outcomes were observed for older patients with AML receiving decitabine + venetoclax for 10 days versus intensive chemotherapy in a propensity ...
The efficacy and safety of venetoclax combined with ...
Our findings demonstrated that the VEN + DEC regimen is both effective and safe for treating elderly patients with AML.
7.
ctv.veeva.com
ctv.veeva.com/study/fhd-286-with-low-dose-weekly-decitabine-venetoclax-in-patients-with-acute-myeloid-leukemiaFHD-286 With Low-Dose Weekly Decitabine/Venetoclax in ...
This is a Phase 1, uncontrolled, single-arm, open-label, nonrandomized, dose escalation, study of Decitabine (DAC)+Venetoclax (VEN)+FHD-286 ...
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