Setmelanotide for Obesity

LT
Overseen ByLindsay T. Fourman, MD
Age: Any Age
Sex: Any
Trial Phase: Phase 2
Sponsor: Massachusetts General Hospital
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Prior Safety DataThis treatment has passed at least one previous human trial
Breakthrough TherapyThis drug has been fast-tracked for approval by the FDA given its high promise

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial explores a treatment called setmelanotide to determine its effectiveness for weight loss in individuals with obesity due to pseudohypoparathyroidism type 1a, a rare condition linked to a specific genetic mutation. The trial will focus on one patient to assess the safety and effectiveness of setmelanotide over six months. Ideal candidates have this rare genetic condition (confirmed GNAS mutation) and obesity, with optimized diabetes and cholesterol management. As a Phase 2 trial, the research measures the treatment's effectiveness in an initial, smaller group of people.

Do I have to stop taking my current medications?

You might need to stop taking certain medications if they could affect the study's results or if their doses might change during the trial. It's best to discuss your current medications with the trial team to see if any adjustments are needed.

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

Research has shown that setmelanotide is generally safe and well-tolerated. In studies with adults and children aged 2 and older, setmelanotide effectively reduces excess body weight and helps maintain weight loss. Some studies reported noticeable reductions in weight and hunger after about a year of treatment.

Regarding side effects, setmelanotide has been linked to some negative reactions, though these are uncommon. In one study, a participant stopped treatment due to a related issue, but such cases appear rare.

Overall, setmelanotide's safety is supported by its approval for treating obesity in patients with specific genetic conditions. This approval indicates that the treatment is considered safe for humans, although individual reactions can vary.12345

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

Setmelanotide is unique because it targets the melanocortin-4 receptor (MC4R) pathway, which plays a critical role in regulating hunger and energy expenditure. Unlike other treatments for obesity related to pseudohypoparathyroidism type 1a, which focus on reducing calorie intake or increasing calorie burning through lifestyle changes and medications, setmelanotide directly addresses the genetic mutations affecting the MC4R pathway. Researchers are excited about this treatment because it offers a more targeted approach, potentially leading to more effective weight loss and better long-term management of obesity in this specific patient group.

What evidence suggests that setmelanotide might be an effective treatment for obesity in pseudohypoparathyroidism type 1a?

Research has shown that setmelanotide can significantly aid weight loss in individuals with obesity. In one study, patients lost 20% of their weight during the first year of treatment. Another study found that setmelanotide improved weight-related health measures and reduced hunger. For children aged 2-5 with rare conditions, setmelanotide led to significant weight loss over a year. While these results are promising, some research suggests that consensus on its effectiveness for all cases of obesity remains elusive. This trial will specifically include patients with obesity related to pseudohypoparathyroidism type 1a.16789

Are You a Good Fit for This Trial?

This trial is for a patient with obesity caused by pseudohypoparathyroidism type 1a (PHP1a) who has a confirmed GNAS gene mutation and whose diabetes and cholesterol are well managed.

Inclusion Criteria

I have PHP1a confirmed by a GNAS gene mutation.
My diabetes and cholesterol are well controlled with treatment.

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive open-label setmelanotide for obesity treatment

6 months
Regular visits for monitoring and assessments

Follow-up

Participants are monitored for safety and effectiveness after treatment

3 months
Follow-up assessments at 3 months

What Are the Treatments Tested in This Trial?

Interventions

  • Setmelanotide

Trial Overview

The study tests setmelanotide, given openly for six months, to see if it helps reduce obesity in one person with PHP1a. The focus is on both effectiveness and safety.

How Is the Trial Designed?

1

Treatment groups

Experimental Treatment

Group I: Patient with pseudohypoparathyroidism type 1aExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Massachusetts General Hospital

Lead Sponsor

Trials
3,066
Recruited
13,430,000+

Citations

NCT07496463 | Setmelanotide to Treat Obesity in a Patient ...

The investigators plan to test the efficacy and safey of 6-months of open-label setmelanotide to treat obesity in a single patient with pseudohypoparathyroidism ...

2.

pubmed.ncbi.nlm.nih.gov

pubmed.ncbi.nlm.nih.gov/40897637/

Real-World Efficacy and Safety of Setmelanotide in Adults ...

Results: Patients experienced a clinically significant weight reduction of 20% from their highest pre-treatment weight within the first year.

Three-Year Setmelanotide Outcomes in Patients with POMC ...

Setmelanotide treatment (Tx) in Phase 3 trials in these populations improved weight-related measures and hunger severity and was well tolerated.

Setmelanotide in patients aged 2–5 years with rare MC4R ...

52 weeks of treatment with the MC4R agonist setmelanotide was associated with meaningful reduction in age-appropriate weight-related measures in paediatric ...

Efficacy and Safety of Setmelanotide in Acquired ...

• Participants previously treated unsuccessfully with a GLP-1 for obesity or concomitantly during the trial with setmelanotide also achieved robust and ...

Safety Profile | IMCIVREE® (setmelanotide) injection | For ...

IMCIVREE is indicated to reduce excess body weight and maintain weight reduction long term in adults and pediatric patients aged 2 years and older.

Efficacy and safety of setmelanotide, a melanocortin-4 ... - PMC

Setmelanotide resulted in significant weight and hunger reductions after 1 year of treatment among patients with BBS; results in patients with ...

Efficacy and safety of setmelanotide, an MC4R agonist, in ...

In the POMC trial, eight (80%) of ten participants achieved at least 10% weight loss compared with baseline at approximately 1 year (p<0·0001 ...

Efficacy and Safety of the MC4R Agonist Setmelanotide in ...

*One participant was not included in the ~1 year measurement due to discontinuation due to treatment-related adverse event. Population includes imputed data ...