Earnings summaries and quarterly performance for Blueprint Medicines.
Executive leadership at Blueprint Medicines.
Kathryn Haviland
President and Chief Executive Officer
Ariel Hurley
Senior Vice President, Finance and Principal Accounting Officer
Becker Hewes
Chief Medical Officer
Christina Rossi
Chief Operating Officer
Debra Durso-Bumpus
Chief People Officer
Fouad Namouni
President, Research and Development
Michael Landsittel
Chief Financial Officer
Percy Carter
Chief Scientific Officer
Philina Lee
Chief Commercial Officer
Tracey McCain
Chief Legal and Compliance Officer
Board of directors at Blueprint Medicines.
Research analysts who have asked questions during Blueprint Medicines earnings calls.
Ami Fadia
Needham & Company, LLC
3 questions for BPMC
Laura Prendergast
Raymond James
2 questions for BPMC
Reni Benjamin
Citizens JMP Securities
2 questions for BPMC
Sudan Loganathan
Stephens Inc.
2 questions for BPMC
Andrew Berens
Leerink Partners
1 question for BPMC
Brad Canino
Stifel Financial Corp.
1 question for BPMC
Colleen Kusy
Robert W. Baird & Co.
1 question for BPMC
David Lebowitz
Citigroup Inc.
1 question for BPMC
Derek Archila
Wells Fargo
1 question for BPMC
Marc Frahm
TD Cowen
1 question for BPMC
Michael Schmidt
Guggenheim Securities
1 question for BPMC
Michael Yee
Jefferies
1 question for BPMC
Paul Jeng
Guggenheim Partners
1 question for BPMC
Peter Lawson
Barclays PLC
1 question for BPMC
Ren Benjamin
Citizen at JPM
1 question for BPMC
Tommie Reerink
Goldman Sachs
1 question for BPMC
Recent press releases and 8-K filings for BPMC.
- Blueprint Medicines Corporation (BPMC) completed its merger with Rothko Merger Sub, Inc., a wholly owned subsidiary of SANOFI's Aventis Inc., on July 17, 2025.
- The acquisition was structured as a tender offer, with shareholders receiving $129.00 per Share in cash plus one non-transferable contractual contingent value right (CVR) per Share.
- Each CVR represents the right to receive contingent payments of up to an aggregate amount of $6.00 per Share in cash upon the achievement of specified milestones.
- The aggregate cash consideration paid by the Purchaser for the shares in the offer and merger was approximately $9.1 billion.
- As a result of the merger, BPMC became a wholly owned subsidiary of Aventis, and its shares will be delisted from Nasdaq.
- Blueprint Medicines showcased a decade of collaboration and data presentations for AYVAKIT®/AYVAKYT® at the 2025 EHA and EAACI congresses, emphasizing its role as a durable standard of care in both indolent and advanced systemic mastocytosis.
- PIONEER three-year results demonstrated sustained symptom improvements through 144 weeks, with a 3 % discontinuation rate due to treatment-related adverse events and a median exposure of three years (some patients treated up to five years).
- PATHFINDER and EXPLORER multi-year analyses showed prolonged overall survival with AYVAKIT versus real-world midostaurin data across all risk categories, validated by the new MARS-R prognostic tool.
- PRISM survey data highlighted the substantial real-world burden of indolent systemic mastocytosis on patients’ physical, social and emotional well-being.
- Sanofi announced it will acquire Blueprint Medicines to expand its portfolio in rare immunological diseases and boost its early-stage immunology pipeline.
- The acquisition includes Blueprint’s approved Ayvakit/Ayvakyt for systemic mastocytosis and advanced candidates like elenestinib and BLU‑808.
- The deal terms feature a cash offer of $129.00 per share (totaling approximately $9.1 billion) plus contingent value rights for potential milestone payments.
- Q1 2025 net product revenues reached $149.4M from AYVAKIT/AYVAKYT sales—including $129.4M in the U.S.—with 61% YoY growth .
- Raised full-year AYVAKIT net product revenue guidance to $700–$720M, supporting a longer-term target of $2B by 2030 .
- Robust growth in patient starts and prescriber expansion driven by targeted allergist initiatives and plans to expand into dermatology and gastroenterology .
- Clinical progress includes advancement in the HARBOR study of elenestinib and initiation of BLU-808 proof-of-concept studies for allergic rhinoconjunctivitis and chronic urticaria, with a sustained favorable safety profile over three years .
- Demonstrated a strong balance sheet with an approximate cash position of $900M, including a $78.7M boost from an equity investment sale .
- AYVAKIT demonstrated strong long-term efficacy and safety in ISM with three-year follow-up data from the PIONEER trial, showing durable symptom improvement and positive effects on bone health.
- BLU-808 displayed a wide therapeutic window and favorable tolerability in Phase 1 trials, supporting its potential as a first-in-class oral wild-type KIT inhibitor.
- Q4 2024 & FY2024 Performance: Reported Q4 total revenue of $146.4M (with $144.1M in net product sales and a $50.0M net loss) and full-year revenue of $508.8M.
- AYVAKIT Growth: Achieved $479.0M in net product revenues in 2024 (including $144.1M in Q4) with 135% YoY growth, driven by strong performance in both US and ex‑US markets.
- 2025 Guidance: Expects global AYVAKIT revenues of $680–710M (approx. 45% YoY growth) with a long-term target of $2B by 2030, alongside an updated systemic mastocytosis franchise peak opportunity of $4B.
- Strategic & Clinical Updates: Highlighted the presentation of 14 abstracts at major conferences, promising Phase 1 healthy volunteer data for BLU-808, and increased investments in R&D, SG&A, commercial infrastructure, and field team expansion supported by a robust cash position of $864M and reduced operating cash burn.
Recent SEC filings and earnings call transcripts for BPMC.
No recent filings or transcripts found for BPMC.