324 Participants NeededMy employer runs this trial

Elritercept for Myelofibrosis and Anemia

(ELRISE MF Trial)

Recruiting at 196 trial locations
Pivotal Trial (Near Approval)This treatment is in the last trial phase before FDA approval
Prior Safety DataThis treatment has passed at least one previous human trial

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial aims to determine if elritercept, a new potential drug, can benefit people with myelofibrosis, a bone marrow disorder, who have anemia while already taking ruxolitinib, a standard treatment. Researchers seek to find out if elritercept can improve anemia, reduce tiredness, and ease daily activities compared to a placebo. The trial will also assess elritercept's effects on bone marrow and the spleen and whether it prompts the body to develop antibodies against it. Individuals diagnosed with myelofibrosis who receive regular blood transfusions might be suitable candidates, especially if they are on a stable dose of ruxolitinib. As a Phase 3 trial, this study represents the final step before FDA approval, offering participants early access to a potentially effective treatment.

Do I have to stop taking my current medications for the trial?

You may need to stop certain medications before joining the trial. Specifically, you cannot have taken certain treatments like androgens, erythropoiesis-stimulating agents, or high-dose corticosteroids within 28 days before starting the trial. However, if you are on a stable dose of ruxolitinib, you can continue taking it.

Is there any evidence suggesting that elritercept is likely to be safe for humans?

Research has shown that elritercept is generally well tolerated by people with myelofibrosis (MF). In patient studies, the most common side effects included low blood platelets, diarrhea, and tiredness, with most being mild to moderate. Specifically, about 29% of patients experienced low blood platelets, and only around 10% had more serious cases. Diarrhea and tiredness were usually mild. These findings suggest that elritercept is safe for many patients, though it may have some side effects.12345

Why do researchers think this study treatment might be promising for myelofibrosis?

Elritercept is unique because it works by targeting the TGF-beta pathway, which is a different approach compared to standard myelofibrosis treatments like JAK inhibitors. This pathway is involved in regulating blood cell production, potentially addressing both myelofibrosis and anemia. Researchers are excited about elritercept because it offers a novel mechanism of action and may improve symptoms in patients who don't respond well to existing therapies. Additionally, its administration as a subcutaneous injection once every four weeks could offer convenience and better adherence compared to more frequent dosing regimens.

What evidence suggests that elritercept might be an effective treatment for myelofibrosis and anemia?

Research has shown that elritercept may help treat anemia in people with myelofibrosis. One study found that 82.8% of patients who did not need blood transfusions experienced an increase in hemoglobin (the protein in red blood cells that carries oxygen) over 12 weeks. Another study revealed that after 36 weeks, 43.5% of patients who regularly needed blood transfusions required them less often. More than half of the patients showed improvements in symptoms and overall health. In this trial, participants will receive either elritercept or a placebo. These findings suggest that elritercept, especially when combined with ruxolitinib, may improve anemia and related symptoms in myelofibrosis patients.25678

Who Is on the Research Team?

SD

Study Director

Principal Investigator

Takeda

Are You a Good Fit for This Trial?

This trial is for adults (18+) with myelofibrosis and anemia who have been taking ruxolitinib at a stable dose for at least 8 weeks. Participants must need regular blood transfusions, be able to understand the study, and be well enough to do most daily activities.

Inclusion Criteria

I am 18 years old or older.
I have been diagnosed with myelofibrosis based on current WHO guidelines.
I have been taking ruxolitinib for my condition for at least 12 weeks on a stable dose.
See 3 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive elritercept or placebo for approximately 36 weeks during the double-blinded treatment period

36 weeks
Visits every 4 weeks

Open-label extension

Participants who received placebo may switch to elritercept, and those on elritercept may continue treatment

Long-term

Follow-up

Participants are monitored for safety and effectiveness after treatment

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • Elritercept

Trial Overview

The study compares elritercept to a placebo in people with myelofibrosis and anemia already on ruxolitinib. It looks at whether elritercept improves anemia, reduces tiredness, helps symptoms, and is safe over time. After 9 months, those on placebo may switch to elritercept.

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Placebo Group

Group I: ElriterceptExperimental Treatment1 Intervention
Group II: PlaceboPlacebo Group2 Interventions

Find a Clinic Near You

Who Is Running the Clinical Trial?

Takeda

Lead Sponsor

Trials
1,255
Recruited
4,219,000+
Dr. Naoyoshi Hirota profile image

Dr. Naoyoshi Hirota

Takeda

Chief Medical Officer since 2020

MD from University of Tokyo

Christophe Weber profile image

Christophe Weber

Takeda

Chief Executive Officer since 2015

PhD in Molecular Biology from Université de Montpellier

Citations

Keros Therapeutics Presents Clinical Data from its Elritercept ...

Increases in hemoglobin were observed in 82.8% (n=24/29) of evaluable non-transfusion dependent patients in both arms over a 12-week period ...

Hematological and clinical improvements with elritercept (KER ...

Conclusions Elritercept as an add on treatment at the RP2D demonstrated clinically meaningful improvements in anemia, thrombocytopenia, spleen ...

NCT05037760 | A Study of Elritercept Alone or Together ...

The main aim of this study is to learn how safe elritercept is and how well it is tolerated when taken alone and in combination with the JAK inhibitor, ...

RESTORE phase II updated results: Elritercept in MF

Outcomes of 38 patients receiving elritercept + ruxolitinib were reported. At 36 weeks, 43.5% of TD patients achieved red blood cell (RBC) transfusion ...

Elritercept Plus Ruxolitinib Demonstrates Favorable Safety ...

Symptom improvement occurred in 89%, and spleen volume reduction in 20 to 22% of patients. After 36 weeks, more than 50% of patients achieved ...

Hematological Improvement and Other Clinical Benefits of ...

Elritercept was generally well tolerated with potential to treat multiple aspects of MF. Observed improvements in Hgb and transfusion burden ...

Elritercept Relieves Anemia and Improves Symptoms in ...

This study evaluated the safety and efficacy of elritercept as monotherapy and in combination with ruxolitinib for patients with myelofibrosis ( ...

NCT04419649 | A Study of Elritercept to Treat Anemia in ...

The main aim of this study is to learn how safe elritercept is and how well adults with anemia associated with lower-risk MDS tolerate treatment with different ...