Silence's Divesiran Demonstrates Durable PV Benefits; Phase 2 Topline Due Aug 2026
Jun 11, 2026, 7:34 AM EDT2 sourcesAI-analyzed
Why it may matterVerify against the original reporting
Positive Phase 1 signals and a near-term Phase 2 catalyst could lift SLN shares, particularly if topline confirms durable phlebotomy reductions and safety. Yet, the lack of a surefire path to approval means upside is contingent on Phase 2 results and execution.
AI summary
What happened, with direct paths to the underlying reporting
Silence Therapeutics reported favorable Phase 1 SANRECO data for divesiran in polycythemia vera, with sustained phlebotomy reductions and improved symptoms and quality of life. Follow-up data show phlebotomy usage stayed low after the final dose, while the Phase 2 SANRECO trial with Q6W and Q12W regimens remains on track for topline results in August 2026, potentially validating a flexible, dosing-favorable therapy.
Phase 1 SANRECO in PV shows symptom/QoL improvements. Phlebotomy reductions persist after final dose.
21 PV patients. 80 pre-treatment phlebotomies vs 5 during active treatment.
16-week follow-up after final dose saw only 4 phlebotomies.
Median time to first phlebotomy: 287 days (n=14).
Phase 2 SANRECO topline due August 2026; Q6W and Q12W dosing on-track.
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