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New injection aims to restore strength in seniors with sarcopenia

NCT ID NCT07668180

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This Phase 2 trial tests an experimental drug called IN-207907 in 100 elderly people with sarcopenia, a condition causing muscle loss and weakness. Participants receive three doses of the drug or a placebo by IV every four weeks. The main goal is to see if the drug improves physical performance, like walking speed and balance.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
IN-207907 injection
What this could lead to
If successful, this could point toward a treatment to improve mobility and reduce frailty in older adults with muscle loss.
What could go wrong
This is an early Phase 2 trial with only 100 participants, so results may not apply to everyone. The drug may not improve physical function more than placebo, and side effects are still being studied.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Phase 2

Tests whether the treatment actually works, and watches for side effects, in a larger group.

Participants

About 100 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Sep 2026

An estimate. Start dates often move.

Expected to finish

Feb 2028

An estimate. End dates often move.

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

65 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Subjects aged ≥ 65 years (for female subjects, those who are medically unable to become pregnant) * Subjects diagnosed with sarcopenia in accordance with the Korean Working Group on Sarcopenia (KWGS) guidelines * Subjects with a body weight of ≥ 35 kg and a body mass index (BMI) of ≥ 15 kg/m² and \< 30 kg/m² * Subjects with a nutritional status screening score of ≥ 8 as assessed by the Mini Nutritional Assessment (MNA) questionnaire Exclusion Criteria: * Subjects with a history of diseases or surgical procedures that may affect physical activity or function * Subjects with underlying muscle disorders, including myopathy or muscular atrophy * Subjects with neuromuscular or neurological disorders * Subjects with uncontrolled diabetes mellitus, severe renal impairment, uncontrolled thyroid disorders, vitamin D deficiency, severe hepatic impairment, severe cardiac disease, uncontrolled hypertension, respiratory disorders * Subjects with clinically significant findings on a 12-lead electrocardiogram (ECG) * Subjects who are positive for active hepatitis B, active hepatitis C, syphilis, or human immunodeficiency virus * Subjects with a history of malignancy within 5 years * Subjects who have received systemic immunosuppressants or immunostimulants * Subjects who have undergone treatment with plasmapheresis within 8 weeks * Subjects who have received treatment with medications prohibited in this clinical trial within 4 weeks * Subjects with hemoglobin levels \< 10 g/dL * Subjects who have undergone surgery requiring general anesthesia within 4 weeks * Subjects who are unable to walk or are physically inactive * Subjects who are participating in or planning to participate in a separate high-intensity program for increasing muscle mass or strength during the clinical trial period * Subjects with severe psychiatric disorders such as major depression, schizophrenia, alcoholism, or drug dependence * Subjects with a score of \< 24 on the Korean version of the Mini Mental State Examination (MMSE-K) * Subjects with known allergies or hypersensitivity to the investigational product or its excipients

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As listed by the trial registrant

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How to take part

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  1. The official record

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  2. A doctor treating you

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