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Somatostatin Agonist
Paltusotine for Acromegaly (PATHFNDR-1 Trial)
Phase 3
Waitlist Available
Research Sponsored by Crinetics Pharmaceuticals Inc.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Confirmed diagnosis of acromegaly and controlled (as measured by IGF-1 ≤1.0×ULN) via stable dose of protocol defined somatostatin receptor ligand therapy
Females must be non-pregnant and non-lactating, and either surgically sterile, post-menopausal, or using effective method(s) of birth control
Must not have
Use of any investigational drug within the past 30 days or 5 half-lives, whichever is longer
Pituitary surgery within 24 weeks prior to Screening or history of pituitary radiation therapy
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Awards & highlights
Pivotal Trial
Summary
This trial is testing paltusotine, a pill that mimics a natural hormone, in patients with acromegaly. The goal is to see if it can help control their high growth hormone levels. Paltusotine is being developed for the treatment of acromegaly and neuroendocrine tumors.
Who is the study for?
Adults diagnosed with acromegaly, previously treated with somatostatin receptor ligand therapy and have their condition under control. Participants must not be pregnant or breastfeeding, should use birth control if necessary, and provide consent. Excluded are those who've used investigational drugs recently, have significant health risks, a history of certain infections or cancer (except some skin cancers), substance abuse within the last year, or specific heart conditions.
What is being tested?
The trial is testing Paltusotine's safety and effectiveness compared to a placebo in adults with acromegaly who were on stable doses of somatostatin receptor ligands. It's randomized and controlled; participants won't know if they're getting the actual drug or a dummy pill.
What are the potential side effects?
Specific side effects for Paltusotine aren't listed here but generally could include digestive issues, changes in blood sugar levels, gallstones symptoms if present before treatment starts, fatigue or allergic reactions.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
My acromegaly is under control with stable medication.
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I am not pregnant or breastfeeding, and I cannot become pregnant or am using birth control.
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My acromegaly is under control with stable medication.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I haven't taken any experimental drugs recently.
Select...
I had pituitary surgery within the last 6 months or have had pituitary radiation therapy.
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I have acromegaly and have not started or have stopped treatment.
Select...
I have been treated with paltusotine before.
Select...
I have painful gallstones.
Select...
I have a history of HIV, hepatitis B, or active hepatitis C.
Select...
I have heart conditions or take medications that affect my heart rhythm.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 5 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
Treatment Details
Awards & Highlights
Pivotal Trial
The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.
Trial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: PaltusotineExperimental Treatment1 Intervention
Group II: PlaceboPlacebo Group1 Intervention
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Paltusotine
2018
Completed Phase 2
~60
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
The most common treatments for Acromegaly include somatostatin analogs such as octreotide, lanreotide, and pasireotide, which work by mimicking the action of somatostatin, a hormone that inhibits the release of growth hormone (GH). By binding to somatostatin receptors on pituitary tumors, these analogs reduce GH secretion and subsequently lower insulin-like growth factor 1 (IGF-1) levels, which are responsible for the symptoms and complications of Acromegaly.
Paltusotine, a nonpeptide somatostatin agonist, operates through a similar mechanism but is orally administered, potentially improving patient compliance and quality of life. Effective management of GH and IGF-1 levels is crucial for preventing the severe complications associated with Acromegaly, such as cardiovascular disease, diabetes, and joint problems.
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Who is running the clinical trial?
Crinetics Pharmaceuticals Inc.Lead Sponsor
11 Previous Clinical Trials
553 Total Patients Enrolled
4 Trials studying Acromegaly
214 Patients Enrolled for Acromegaly
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- My acromegaly is under control with stable medication.I haven't taken any experimental drugs recently.I had pituitary surgery within the last 6 months or have had pituitary radiation therapy.I have not had cancer, except for certain skin cancers, in the last 5 years.I have acromegaly and have not started or have stopped treatment.I have been treated with paltusotine before.I have painful gallstones.You have had a problem with drinking too much alcohol or using drugs in the past year.I am 18 years old or older.I am not pregnant or breastfeeding, and I cannot become pregnant or am using birth control.I have a history of HIV, hepatitis B, or active hepatitis C.I have heart conditions or take medications that affect my heart rhythm.I haven't taken certain hormone therapies for my condition in the weeks before screening.My acromegaly is under control with stable medication.
Research Study Groups:
This trial has the following groups:- Group 1: Paltusotine
- Group 2: Placebo
Awards:
This trial has 1 awards, including:- Pivotal Trial - The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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