Clinical Trials
We thoughtfully design and conduct clinical trials to evaluate the safety and efficacy of our therapies, working cross-functionally and collaboratively to ensure our trials are designed and executed with a focus on compliance. We conduct trials in an ethical manner and maintain the highest standards of clinical trial quality to ensure the integrity of our clinical data. We also comply with all laws, regulations, and industry codes, and remain steadfast in our commitment to following good clinical practice.
Importantly, we ensure the patients who participate in our clinical trials do so on a voluntary and informed basis and that the potential risks and benefits from our trials are considered appropriate. This means we make sure our trials, including protocols and informed consent forms, are reviewed and approved by Institutional Review Boards/Independent Ethics Committees before participants are screened for potential inclusion.
How we do it
- When choosing clinical trial investigators and sites, we substantiate their medical expertise and clinical research experience to ensure there is no bias or perception of bias.
- We share clinical trial results with trial investigators, healthcare professionals, and the general public in a timely and accurate manner, and in accordance with relevant rules, regulations, and industry codes.
- We ensure the integrity of clinical trial data collected during the study and oversee data generation and collection to safeguard against fraudulent data or inappropriate clinical site practices.
Did you know?
Insmed takes seriously its responsibility to safeguard the health information shared with us by clinical trial participants. The third-party suppliers that support our clinical trials must uphold the same responsibility. Insmed and our suppliers take care when collecting, reviewing, or using health information, use it only for purposes related to the trial, and protect its security at all times.
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