SFDA Grants Breakthrough Designation to Bemlayo for Obesity/Overweight
Summary
The Saudi Food and Drug Authority (SFDA) has granted Eli Lilly's drug Bemlayo (Orforglipron) Breakthrough designation. This designation expedites the review process for innovative treatments for serious diseases but does not constitute marketing authorization.
What changed
The Saudi Food and Drug Authority (SFDA) has granted Eli Lilly and Company's drug Bemlayo (Orforglipron) a Breakthrough designation. This designation allows the drug, indicated for adults with obesity or overweight with at least one weight-related comorbidity, to be submitted and reviewed under the SFDA's Breakthrough Track, which aims to expedite access to innovative treatments for serious diseases where existing therapies may be inadequate.
This designation is not a marketing authorization; a final decision on registration will follow a full technical and scientific evaluation of the complete registration dossier. The Breakthrough Medicines Program requires drugs to have completed clinical trials demonstrating promising efficacy and safety, offer a significant therapeutic advantage, target serious or life-threatening conditions, and exhibit a positive benefit-risk balance. The product must also not be registered with any other regulatory authority at the time of application.
What to do next
- Monitor SFDA's evaluation of Bemlayo's registration dossier.
- Review SFDA's Breakthrough Medicines Program guide for potential future applications.
Source document (simplified)
The Saudi Food and Drug Authority (SFDA) has granted Eli Lilly Breakthrough designation to Bemlayo (Orforglipron), which is indicated as an adjunct to healthy diet and physical activity to reduce excess body weight and maintain weight reduction long term in adults with obesity or adults with overweight in the presence of at least one weight-related comorbid condition.
Registration is Subjected to Full Scientific Evaluation
The SFDA emphasizes that this designation allows Bemlayo to be submitted and reviewed under the Breakthrough Track, subject to specific regulatory controls and mechanisms. This designation does not constitute a marketing authorization of the drug in Saudi Arabia. A final decision regarding registration will be announced following a full technical and scientific evaluation of the complete registration dossier.
The SFDA Breakthrough Medicine Program Expedites Access to Targeted Treatments
The Program aims to expedite access to innovative and effective treatments for serious diseases where existing therapies may be inadequate. To qualify for this designation, a drug must have completed clinical trials demonstrating promising efficacy and safety, offer a significant therapeutic advantage over current options, target serious or life-threatening conditions, and exhibit a positive benefit-risk balance. Notably, the product should not be registered with any other regulatory authority at the time of application.
For further information about the Breakthrough Medicines Program, please refer to the guide available on the SFDA website:
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