ASC30 for Obesity
Trial Summary
What is the purpose of this trial?
This is a phase I, randomized, double-blind, placebo-controlled, single and multiple ascending dose study to evaluate the safety, tolerability, and pharmacokinetics of ASC30 Tablets in participants with obesity.
Do I have to stop taking my current medications for the trial?
The trial protocol does not specify if you need to stop taking your current medications. However, since the trial excludes participants with certain health conditions, it's possible that some medications might not be allowed. Please consult with the trial coordinator for more details.
What data supports the idea that ASC30 for Obesity is an effective treatment?
The available research does not provide specific data on ASC30 for Obesity, so we cannot determine its effectiveness from the information given. The studies focus on other aspects of obesity treatment, such as the importance of long-term support and the challenges in recognizing and documenting obesity. Without direct data on ASC30, we can't compare it to other treatments or confirm its effectiveness.12345
What safety data exists for ASC30 treatment for obesity?
Eligibility Criteria
This trial is for individuals with obesity who are interested in testing a new treatment. Participants must meet certain health criteria to join, but specific inclusion and exclusion details aren't provided here.Inclusion Criteria
Exclusion Criteria
Treatment Details
Interventions
- ASC30 (Anti-obesity Medication)
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Who Is Running the Clinical Trial?
Ascletis Pharma (China) Co., Limited
Lead Sponsor