HMPL-689 for Lymphoma
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial tests a new treatment called HMPL-689, a potential drug, to determine its safety and tolerability in people with certain types of lymphoma, a cancer affecting the immune system. It targets patients whose cancer has returned or has not responded to other treatments. Participants must have a confirmed lymphoma diagnosis and no remaining standard treatment options. The trial aims to assess the body's response to different doses and gather information on the drug's behavior in the body. As a Phase 1 trial, this research seeks to understand how the treatment works in people, offering participants the opportunity to be among the first to receive this new drug.
Do I have to stop taking my current medications for the HMPL-689 trial?
The trial requires that you stop certain medications before participating. You must not have used cancer therapy within 3 weeks, GCSF within 7 days, steroid therapy within 7 days, strong CYP3A4 inducers within 2 weeks, or have had a transplant within 6 months before starting the trial. Additionally, you cannot use medications known to cause QT prolongation.
Is there any evidence suggesting that HMPL-689 is likely to be safe for humans?
Research has shown that HMPL-689 is generally safe for people with lymphoma. In earlier studies, patients took HMPL-689 daily without major problems. The treatment had a manageable safety profile, with serious side effects being rare. Many patients, including those with recurrent or treatment-resistant lymphoma, responded well to HMPL-689. These results suggest that HMPL-689 could be a safe option for those considering participation in this trial.12345
Why do researchers think this study treatment might be promising?
HMPL-689 is unique because it targets a specific enzyme called PI3Kδ, which plays a crucial role in the growth and survival of lymphoma cells. Most current treatments for lymphoma, like chemotherapy or monoclonal antibodies, attack cancer cells more broadly, which can lead to more side effects. By focusing specifically on PI3Kδ, HMPL-689 might offer a more precise approach, potentially reducing side effects while effectively targeting the cancer. Researchers are excited about this targeted action because it represents a shift towards more personalized and potentially safer cancer therapies.
What evidence suggests that HMPL-689 might be an effective treatment for lymphoma?
Research has shown that HMPL-689 may help treat lymphoma that has returned or hasn't responded to other treatments. In one study, about 53% of patients experienced improvement with this treatment. It is also considered safe and manageable for patients. Early studies suggest that HMPL-689 could work well on its own, especially in challenging cases of B-cell lymphoma. Evidence indicates that HMPL-689 could benefit those who haven't had success with other treatments.12345
Who Is on the Research Team?
Claudia Huang
Principal Investigator
Hutchmed Limited
Nilanjan Ghosh, MD
Principal Investigator
Atrium Health Levine Cancer Institute
Jonathan B Cohen, MD
Principal Investigator
Emory Winship Cancer Institute
Are You a Good Fit for This Trial?
This trial is for patients with certain types of lymphoma that have relapsed or are not responding to standard treatments. Participants should be in relatively good physical condition (ECOG status 0 or 1) and expected to live more than 24 weeks. They must not have severe organ dysfunction, recent major surgery, heart issues like congestive heart failure, a history of significant liver disease, or any other condition that could interfere with the study.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Dose Escalation
Participants receive escalating doses of HMPL-689 to determine the maximum tolerated dose (MTD) and/or recommended phase 2 dose (RP2D)
Dose Expansion
Participants receive HMPL-689 at the RP2D to further characterize safety and explore preliminary anti-tumor activity
Follow-up
Participants are monitored for safety and effectiveness after treatment
What Are the Treatments Tested in This Trial?
Interventions
- HMPL-689
Find a Clinic Near You
Who Is Running the Clinical Trial?
Hutchison Medipharma Limited
Lead Sponsor
Dr. Weiguo Su
Hutchison Medipharma Limited
Chief Executive Officer since 2022
PhD in Chemistry from Harvard University, BSc in Chemistry from Fudan University
Dr. Karen Atkin
Hutchison Medipharma Limited
Chief Medical Officer since 2023
MD from Harvard Medical School
Hutchmed
Lead Sponsor