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FT538 for Acute Myeloid Leukemia
Study Summary
This trial is testing a new cancer drug called FT538. The first part of the trial is to find the best dose of the drug. The second part is to see if the drug works better when used with other drugs that are already used to treat cancer.
- Acute Myeloid Leukemia
- Multiple Myeloma
Timeline
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Trial Design
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Who is running the clinical trial?
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- You are allergic to albumin (human) or DMSO.You have been diagnosed with one of the following conditions according to the treatment plan:This study is specifically for patients with relapsed or refractory acute myeloid leukemia (AML) who will be treated with the medication FT538 alone (Regimen A).You have cancer that has spread to your brain or spinal cord and is actively causing problems.You are being considered for Treatment Regimens B or C, which involve using a combination of drugs called FT538 and a type of medication called monoclonal antibodies for patients with relapsed or refractory multiple myeloma.For Regimen C, you have multiple myeloma that has come back or gotten worse after treatment with proteasome inhibitors and immunomodulatory therapy.Your organs are not functioning properly, as determined by the study guidelines.You have a serious heart condition that is defined by the study's rules.You have had a non-cancerous disease affecting your brain or nervous system, such as stroke, epilepsy, or neurodegenerative disease, or have taken medications for these conditions within the past 2 years.For regimen B, you must have multiple myeloma that has come back or gotten worse after trying at least two different treatments, including a drug that blocks proteasomes and a drug that helps regulate the immune system.
- Group 1: FT538 Monotherapy
- Group 2: FT538 in Combination with Daratumumab
- Group 3: FT538 in Combination with Elotuzumab
- Approved for 20 Other Conditions - This treatment demonstrated efficacy for 20 other conditions.
- All Individual Drugs Already Approved - Therapies where all constituent drugs have already been approved are likely to have better-understood side effect profiles.
- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
Are researchers still enrolling patients for this trial?
"The clinical trial is currently looking for participants. Based on the information found on clinicaltrials.gov, the trial was first posted on October 17th, 2020 and was most recently edited on May 19th, 2022."
What are the conditions that FT538 is known to improve?
"FT538 is often used to treat lung cancer, but it has also shown efficacy against other diseases like multiple sclerosis, leukemia, myelocytic, acute, and amyloidosis."
Is FT538 able to be legally prescribed by medical doctors in the United States?
"Because this is an early-stage trial, there is limited data on both safety and efficacy. As a result, our team has given FT538 a score of 1."
Could you give me the total patient count for this clinical trial?
"One hundred and five research subjects are required to partake in this clinical trial. The trial's locations include the Colorado Blood Cancer Institute in Denver, Colorado and St. David's South Austin Medical Center in Austin, Texas."
Are there other similar medical experiments underway that use FT538?
"At this time, 1074 different clinical trials are investigating the efficacy of FT538 with 192 of those in Phase 3. A large majority of these tests are being conducted in Philadelphia, but there are a total of 34429 locations running FT538 trials."
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