Analyst Summary
- Theratechnologies has resumed distribution of EGRIFTA SV (tesamorelin for injection).
- The FDA allowed the company to release two recently manufactured batches of EGRIFTA SV.
- The product is ready for immediate shipment to network pharmacies.
- The FDA’s review of the Prior Approval Supplement is ongoing with a goal date of April 18, 2025.
Opportunities and Risks
- Opportunity: PAS will be approved by the FDA.
- Risk: FDA’s review of the PAS not being completed by April 18, 2025.
- Risk: Non-approval of the PAS.
- Risk: A decrease in demand for EGRIFTA SV ® due to the recent shortage adversely impacting the resumption of the commercialization of EGRIFTA SV ® .