Laekna, Inc. ((HK:2105)) announced an update on their ongoing clinical study.
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Laekna, Inc. (HK:2105) is conducting a Phase I clinical study titled ‘A Randomized, Double-Blind, Placebo-Controlled, Single and Multiple Dose Escalation Phase I Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of LAE102 Injection in Healthy and Overweight/Obese Subjects.’ The study aims to assess the safety, tolerability, and pharmacokinetics of LAE102 injections in both healthy and overweight/obese participants, while also evaluating its preliminary pharmacodynamic effects in overweight/obese subjects. This research is significant as it could lead to new treatments for obesity-related conditions.
The intervention being tested is LAE102, administered both intravenously and subcutaneously. It is designed to explore the drug’s safety and effectiveness in different dosages and administration methods, with the ultimate goal of treating obesity-related health issues.
The study is interventional, with a randomized allocation and a sequential intervention model. It employs a quadruple masking approach, meaning that the participant, care provider, investigator, and outcomes assessor are all blinded to the treatment allocation. The primary purpose of the study is treatment-focused.
The study began on June 3, 2024, with the primary completion date yet to be announced. The most recent update was submitted on April 7, 2025. These dates are crucial for tracking the study’s progress and anticipating future developments.
The ongoing study could potentially influence Laekna’s stock performance positively if the results indicate a breakthrough in obesity treatment. Investors are likely to keep a close watch on this study, as positive outcomes could enhance Laekna’s market position. Competitors in the obesity treatment market may also be impacted, depending on the study’s results.
The study is currently recruiting, with further details available on the ClinicalTrials portal.