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Analyst Price Targets — REPL

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DateAnalystFirmTargetPrice @ PostSourceHeadline
June 30, 2026 11:46 amWedbush$9.00$11.20TheFly Replimune price target raised to $9 from $6 at Wedbush
June 30, 2026 8:36 amEvan SeigermanBMO Capital$16.00$11.20TheFly Replimune upgraded to Outperform from Market Perform at BMO Capital
February 5, 2026 11:49 amPiper Sandler$14.00$7.00TheFly Replimune price target raised to $14 from $13 at Piper Sandler
November 3, 2025 9:23 amEvan SeigermanBMO Capital$11.00$9.73TheFly Replimune upgraded to Market Perform from Underperform at BMO Capital
October 27, 2025 10:17 amH.C. Wainwright$12.00$8.80TheFly Replimune upgraded to Buy from Neutral at H.C. Wainwright
October 20, 2025 1:05 pmWedbush$18.00$9.15TheFly Wedbush upgrades Replimune to Outperform amid second BLA review
January 22, 2025 2:41 pmEvan SeigermanBMO Capital$27.00$13.09TheFly Replimune price target raised to $27 from $18 at BMO Capital
December 3, 2024 8:58 pmRoger SongJefferies$19.00$14.48StreetInsider Replimune Group (REPL) PT Raised to $19 at Jefferies
June 7, 2024 6:07 amRobert BurnsH.C. Wainwright$17.00$7.11TheFly Replimune Group price target raised to $17 from $12 at H.C. Wainwright
June 4, 2024 9:51 amPeter LawsonBarclays$13.00$5.37StreetInsider Barclays Reiterates Overweight Rating on Replimune Group (REPL)

Latest News for REPL

Replimune: Stock Buoyant On Third Try At RP1 Approval - FDA AdCom May Be Crucial

Replimune Group, Inc. faces a pivotal FDA AdCom for RP1 after two prior rejections, with a final FDA approval decision expected August 2, 2026. RP1 demonstrated a 34% ORR and median overall survival of 32.9 months in anti-PD-1-failed melanoma, but trial design concerns persist. REPL stock has surged over 135% since April as FDA leadership changes and collaborative dialogue opened a path for BLA resubmission.

Seeking Alpha • Jun 30, 2026
Replimune Announces FDA Acceptance of RP1 Biologics License Application Resubmission for Advanced Melanoma

WOBURN, Mass., June 26, 2026 (GLOBE NEWSWIRE) -- Replimune Group, Inc. (NASDAQ: REPL), a clinical-stage biotechnology company pioneering the development of novel oncolytic immunotherapies, announced today that the U.S. Food and Drug Administration (FDA) has accepted for review the resubmission of the Biologics License Application (BLA) for RP1 (vusolimogene oderparepvec) in combination with nivolumab for the…

GlobeNewsWire • Jun 26, 2026

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