ELA026 for Lymphoma
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial tests a new treatment called ELA026, a potential drug for individuals with a type of lymphoma that hasn't responded to other treatments. As a Phase 1 study, the researchers aim to determine the treatment's safety and identify the correct dose. They are testing three different dose levels to find the most effective one. Individuals who have tried at least two treatments for their lymphoma and still have measurable disease may qualify. Participants in this Phase 1 trial will be among the first to receive this new treatment, aiding researchers in understanding its effects in people.
Do I need to stop my current medications for the ELA026 trial?
The trial does not specify if you need to stop taking your current medications. However, you cannot participate if you are receiving or planning to start certain immunotherapies or immune cell therapies.
Is there any evidence suggesting that ELA026 is likely to be safe for humans?
Research shows that ELA026 is generally well-tolerated by patients. In studies on secondary hemophagocytic lymphohistiocytosis (sHLH), ELA026 proved safe, with manageable side effects. All patients in these studies responded well to the treatment and had improved survival chances after two months. While these results are encouraging, ELA026 remains in the early stages of testing for lymphoma. More research is needed to fully understand its safety for this specific condition.12345
Why do researchers think this study treatment might be promising for lymphoma?
ELA026 is unique because it offers a fresh approach to treating lymphoma. Unlike traditional treatments like chemotherapy and radiation, which attack cancer cells broadly, ELA026 targets specific pathways involved in lymphoma cell growth. This targeted mechanism could mean fewer side effects and more effective outcomes for patients. Researchers are excited because this precision approach has the potential to improve the quality of life for those with lymphoma by minimizing the collateral damage to healthy cells.
What evidence suggests that ELA026 might be an effective treatment for lymphoma?
Research has shown that ELA026, a monoclonal antibody, offers promising results for certain inflammation-related conditions. In earlier studies with similar conditions, ELA026 helped all patients respond positively and improved their survival rates after two months. Patients generally tolerated the treatment well, experiencing manageable side effects. ELA026 targets and reduces specific cells that cause inflammation, improving symptoms and patient outcomes. While these results are encouraging, the treatment is still under study for its effectiveness in treating lymphoma specifically. Participants in this trial will receive varying doses of ELA026 to evaluate its safety and efficacy in lymphoma treatment.12346
Are You a Good Fit for This Trial?
This trial is for adults (18 or older) with certain T-cell or NK-cell cancers that have come back or not responded to previous treatments. Participants must be well enough to do daily activities, have measurable disease, and a life expectancy of over 6 months.Inclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants receive ELA026 for up to 6 cycles (24 weeks) to evaluate dosing regimens
Optional extension
Participants experiencing ongoing clinical benefits may continue treatment for up to an additional 6 cycles
Safety follow-up
Participants are monitored for safety 28 days after the last dose of study treatment
Survival follow-up
Participants are monitored for survival up to 2 years from the end of treatment
What Are the Treatments Tested in This Trial?
Interventions
- ELA026
Trial Overview
The study is testing ELA026, a new treatment, in people whose T/NK cell cancers did not improve with earlier therapies. It’s an early-phase trial happening at multiple centers.
How Is the Trial Designed?
3
Treatment groups
Experimental Treatment
Starting dose level
Dose level below Starting Dose Level
Dose level above Starting Dose Level
Find a Clinic Near You
Who Is Running the Clinical Trial?
Electra Therapeutics Inc.
Lead Sponsor
Citations
1.
ashpublications.org
ashpublications.org/blood/article/144/Supplement%201/805/530633/ELA026-a-Monoclonal-Antibody-Targeting-SignalELA026, a Monoclonal Antibody Targeting Signal Regulatory ...
Conclusion: Data suggest ELA026 is well-tolerated to date in sHLH patients and results in a 100% response rate and improved 2-month survival ...
2.
electra-therapeutics.com
electra-therapeutics.com/electra-therapeutics-presents-late-breaking-clinical-data-at-eha2024-from-ongoing-phase-1b-study-of-ela026-in-secondary-hemophagocytic-lymphohistiocytosis-shlh/Electra Therapeutics Presents Late-Breaking Clinical Data ...
In treatment naive mHLH patients, ELA026 achieved a 100% overall response rate (ORR) by week 4 and improved survival at two months compared to ...
A PHASE 1B STUDY OF ELA026 IN PATIENTS WITH ... - PMC
Biomarker evidence of improvement is defined as monocyte depletion ≥75% from baseline to the end of the dosing interval and serum ferritin reduction ≥20% ...
NCT07465835 | A Study of ELA026 in Participants With ...
A type of eligibility criteria that indicates whether people who do not have the condition/disease being studied can participate in that clinical study. ... An ...
5.
mdanderson.org
mdanderson.org/newsroom/ash--monoclonal-antibody-therapy-improves-survival-in-cancer-associated-hyper-inflammatory-disorder.h00-159703068.htmlMonoclonal antibody therapy improves survival in cancer ...
The first-in-class monoclonal antibody, ELA026, experienced a 100% response rate and an improved survival rate at two months, according to researchers.
The surpass trial: a phase 2/3 registrational trial of ELA026 ...
In the phase 1b portion of ELA026-CP002 (NCT05416307), ELA026 demonstrated an encouraging safety profile and 100% survival rate at 8-weeks ...
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