84 Participants NeededMy employer runs this trial

ELA026 for Lymphoma

Recruiting at 5 trial locations
CT
Overseen ByClinical Trials Electra Clinical Trials Information
Age: 18+
Sex: Any
Trial Phase: Phase 1
Sponsor: Electra Therapeutics Inc.
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

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

I am able to care for myself and do light activities.
I am 18 or older and my T-cell cancer has come back or not responded to treatment.
* Presence of measurable disease by clinical examination, radiologic imaging (computed tomography, magnetic resonance imaging, or whole body FDG-PET scans), and/or in bone marrow aspirate/biopsy
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Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

4 weeks

Treatment

Participants receive ELA026 for up to 6 cycles (24 weeks) to evaluate dosing regimens

24 weeks

Optional extension

Participants experiencing ongoing clinical benefits may continue treatment for up to an additional 6 cycles

24 weeks

Safety follow-up

Participants are monitored for safety 28 days after the last dose of study treatment

4 weeks

Survival follow-up

Participants are monitored for survival up to 2 years from the end of treatment

Up to 2 years

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

Group I: Level 0 ArmExperimental Treatment1 Intervention
Group II: Level -1 ArmExperimental Treatment1 Intervention
Group III: Level +1 ArmExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Electra Therapeutics Inc.

Lead Sponsor

Trials
2
Recruited
250+

Citations

ELA026, 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 ...

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 ...

Monoclonal 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 ...