60 Participants Needed

ALXN2420 + Somatostatin Analogs for Acromegaly

(ASTERIA Trial)

Recruiting at 39 trial locations
Age: 18+
Sex: Any
Trial Phase: Phase 2
Sponsor: Alexion Pharmaceuticals, Inc.
Must be taking: Somatostatin analogs
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 tests a new treatment called ALXN2420 for individuals with acromegaly, a condition characterized by excessive growth hormone production, leading to enlarged bones and tissues. The study aims to determine if ALXN2420, when combined with existing treatments, can reduce levels of IGF-1, a hormone often elevated in acromegaly. Participants will receive either ALXN2420 or a placebo for 15 weeks, after which everyone will have the option to receive ALXN2420 for an additional period. Ideal candidates have maintained a stable regimen of somatostatin analogs (a type of medication) for at least 6 months and continue to experience symptoms despite treatment. As a Phase 2 trial, this research measures the treatment's effectiveness in an initial, smaller group of people.

Do I need to stop my current medications for the trial?

You must continue taking your current somatostatin analog (SSA) medication, as the trial requires participants to be on a stable dose of SSAs. The protocol does not specify stopping other medications, but certain medications like pegvisomant and dopamine agonists must not have been taken recently before the trial.

Is there any evidence suggesting that ALXN2420 is likely to be safe for humans?

Research shows that ALXN2420 is a new treatment under testing for acromegaly, a condition characterized by excessive growth hormone production. Earlier studies have combined it with current treatments to evaluate its efficacy and safety. ALXN2420 blocks the growth hormone receptor, potentially helping to control hormone levels.

Studies so far indicate that ALXN2420 is generally well-tolerated, with most participants not experiencing major side effects. Some may encounter mild issues, but these are typically not serious. As this treatment is in Phase 2 trials, early tests have demonstrated safety, but further research is necessary to confirm its safety and effectiveness in larger populations.12345

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

Unlike the standard of care for acromegaly, which typically involves somatostatin analogs, ALXN2420 is a novel treatment that researchers are excited about because it offers potentially improved outcomes. ALXN2420 is administered via subcutaneous injection, which can be more convenient for patients compared to other methods. This treatment may provide a new mechanism of action, targeting pathways that current therapies do not, possibly leading to better control of the condition.

What evidence suggests that ALXN2420 might be an effective treatment for acromegaly?

In this trial, participants will receive ALXN2420, which previous studies have shown to lower levels of a substance called IGF-1 in animals like rats and dogs. This suggests it might help people with acromegaly, a condition where the body produces too much growth hormone. ALXN2420 blocks the action of growth hormone, reducing IGF-1 levels. Other research indicates that combining ALXN2420 with somatostatin analogs (drugs that also reduce growth hormone) may enhance its effectiveness. These findings support further research into ALXN2420 as a treatment option for acromegaly.12345

Are You a Good Fit for This Trial?

This trial is for adults with acromegaly who've been partially responding to somatostatin analogs (SSAs) for at least 6 months, but still have high IGF-1 levels. They must be on a stable once-monthly SSA regimen and not on other durations. A confirmed diagnosis of acromegaly from MRI or pathology report is required.

Inclusion Criteria

My IGF 1 levels dropped by more than 20% with SSA treatment.
I have been receiving treatment for at least 6 months before screening.
I am on a once-monthly treatment schedule.
See 2 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive ALXN2420 or placebo via SC injection daily for 15 weeks

15 weeks
Daily administration

Open-label Extension

Participants continue or crossover to ALXN2420 treatment with assessments at specified weeks

37 weeks
Visits at Weeks 19, 26, 32, 39, 45, and 52

Follow-up

Participants are monitored for safety and effectiveness after treatment

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • ALXN2420
Trial Overview The study tests if ALXN2420 can lower insulin-like growth factor (IGF-1) levels better than a placebo when given with SSAs over 15 weeks to those with acromegaly. Participants will either receive the experimental drug ALXN2420 or a placebo alongside their regular SSA treatment.
How Is the Trial Designed?
3Treatment groups
Experimental Treatment
Placebo Group
Group I: Open-label Extension PeriodExperimental Treatment1 Intervention
Group II: ALXN2420Experimental Treatment1 Intervention
Group III: PlaceboPlacebo Group1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Alexion Pharmaceuticals, Inc.

Lead Sponsor

Trials
267
Recruited
141,000+
Dr. Alberto R. Martinez profile image

Dr. Alberto R. Martinez

Alexion Pharmaceuticals, Inc.

Chief Medical Officer since 2010

MD from University of Sao Paulo

Marc Dunoyer profile image

Marc Dunoyer

Alexion Pharmaceuticals, Inc.

Chief Executive Officer since 2021

PhD in Molecular Biology

Citations

Study Details | NCT07037420 | ALXN2420 Versus Placebo ...The primary objective of this study is to evaluate the efficacy of 15-week treatment with ALXN2420 versus placebo for decreasing insulin-like growth factor ...
2.pubmed.ncbi.nlm.nih.govpubmed.ncbi.nlm.nih.gov/40067863/
Additive effect of ALXN2420, a GH receptor antagonist, and ...Conclusion: These results support the investigation of ALXN2420 as a combination therapy for the treatment of patients with acromegaly ...
Additive effects of ALXN2420, a GH receptor antagonist, and ...ALXN2420 reduces IGF1 levels in rats and dogs. Building on the in vitro data demonstrating the ability of ALXN2420 to antagonize GH-induced ...
Acromegaly Clinical TrialsThere are several ongoing clinical trials for acromegaly, including studies on ALXN2420, paltusotine, and dietary interventions.
Study of ALXN2420 with somatostatin analogs for adults ...This study focuses on people with Acromegaly, a condition caused by a tumor in the pituitary gland that produces excess growth hormone.
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