Leuprolide for Precocious Puberty
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial tests whether the drug Leuprolide Mesylate, a hormone therapy, is safe and effective for children with central precocious puberty (early puberty due to hormone issues). Participants will receive two injections of the drug, six months apart, to determine its effectiveness in managing their condition. Suitable candidates are children aged 2 to 8 for girls and 2 to 9 for boys, who show early signs of puberty, such as breast development or increased testicle size, and have not started other treatments for this condition. As a Phase 3 trial, this study represents the final step before FDA approval, offering participants a chance to contribute to a potentially groundbreaking treatment.
Will I have to stop taking my current medications?
The trial does not specify if you need to stop taking your current medications. However, if you are currently using medications associated with seizures or convulsions, you may need to stop them as they are excluded from the trial.
Is there any evidence suggesting that Leuprolide Mesylate is likely to be safe for humans?
Research has shown that Leuprolide Mesylate, a treatment for early puberty, is generally safe. Studies have found that its six-month injection has a safety record similar to other treatments, with manageable and expected side effects. For instance, a long-term study found that Leuprolide Mesylate does not affect body weight or cause early puberty to return later. It can also help children grow taller as adults. Overall, children with early puberty tolerate Leuprolide Mesylate well.12345
Why do researchers think this study treatment might be promising for precocious puberty?
Leuprolide Mesylate is unique because it offers a potentially more convenient dosing schedule for managing central precocious puberty. Unlike standard treatments that often require monthly injections, this new formulation only needs to be administered twice in a year, with doses given six months apart. This can significantly reduce the treatment burden for young patients and their families, making it an exciting advancement in treatment options. Researchers are optimistic that this less frequent dosing will maintain effectiveness while improving patient compliance and quality of life.
What evidence suggests that Leuprolide Mesylate might be an effective treatment for precocious puberty?
Research shows that Leuprolide Mesylate effectively treats early puberty, known as central precocious puberty (CPP). Studies on similar versions, such as the 1-month depot, have demonstrated positive effects on growth and help maintain normal adult height. After treatment, patients typically return to a normal puberty process, and girls often have regular periods by age 12. In this trial, participants will receive a 6-month depot version of Leuprolide, which other studies have found to effectively control hormone levels and growth in children with CPP. Overall, leuprolide treatments have safely managed early puberty symptoms, supporting their use for this condition.34678
Who Is on the Research Team?
Bassem Elmankabadi
Principal Investigator
Foresee Pharma
Are You a Good Fit for This Trial?
This trial is for young children with early onset puberty: girls aged 2-8 and boys aged 2-9 who have been diagnosed with central precocious puberty (CPP) within the last year. They should not have had previous treatment for CPP, be able to participate in the study, and have parental consent.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants receive two injections of FP-001 42 mg, six months apart
Follow-up
Participants are monitored for safety and effectiveness after treatment
What Are the Treatments Tested in This Trial?
Interventions
- Leuprolide Mesylate
Leuprolide Mesylate is already approved in United States, European Union, Canada, Japan for the following indications:
- Prostate cancer
- Breast cancer
- Endometriosis
- Uterine fibroids
- Central precocious puberty
- Prostate cancer
- Breast cancer
- Endometriosis
- Uterine fibroids
- Central precocious puberty
- Prostate cancer
- Breast cancer
- Endometriosis
- Uterine fibroids
- Central precocious puberty
- Prostate cancer
- Breast cancer
- Endometriosis
- Uterine fibroids
- Central precocious puberty
Find a Clinic Near You
Who Is Running the Clinical Trial?
Foresee Pharmaceuticals Co., Ltd.
Lead Sponsor
Changchun GeneScience Pharmaceuticals Co., Ltd.
Industry Sponsor
QPS
Collaborator
QPS Holdings LLC
Industry Sponsor
Changchun GeneScience Pharmaceutical Co., Ltd.
Industry Sponsor
Dr. Lei Jin
Changchun GeneScience Pharmaceutical Co., Ltd.
Chief Executive Officer
PhD
Dr. Yuanfeng Xia
Changchun GeneScience Pharmaceutical Co., Ltd.
Chief Medical Officer
MD
GeneScience Pharmaceuticals Co., Ltd.
Industry Sponsor