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Spark Therapeutics to Host Conference Call on Tuesday, May 8 at 8:30 a.m. ET to Discuss First Quarter Results and Recent Business Highlights
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Spark Therapeutics to Host Conference Call on Tuesday, May 8 at 8:30 a.m. ET to Discuss First Quarter Results and Recent Business Highlights
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Spark Therapeutics to Host Conference Call on Tuesday, May 8 at 8:30 a.m. ET to Discuss First Quarter Results and Recent Business Highlights
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Spark Therapeutics (ONCE) Sells Priority Review Voucher for $110 Million
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Spark Therapeutics Sells Priority Review Voucher for $110 Million
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Spark Therapeutics Sells Priority Review Voucher for $110 Million
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Spark Therapeutics to Participate in Multiple Conferences in March
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Spark Therapeutics to Participate in Multiple Conferences in March
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Spark Therapeutics to Participate in Multiple Conferences in March
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Spark Therapeutics Reports 2017 Financial Results and Recent Business Progress
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Spark Therapeutics Reports 2017 Financial Results and Recent Business Progress
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Spark Therapeutics to Host Conference Call on Tuesday, Feb. 20 at 8:30 a.m. ET to Discuss 2017 Results and Recent Business Highlights
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Spark Therapeutics to Host Conference Call on Tuesday, Feb. 20 at 8:30 a.m. ET to Discuss 2017 Results and Recent Business Highlights
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Spark Therapeutics to Host Conference Call on Tuesday, Feb. 20 at 8:30 a.m. ET to Discuss 2017 Results and Recent Business Highlights
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Spark Therapeutics to Participate in Multiple Conferences in February
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Spark Therapeutics to Participate in Multiple Conferences in February
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Spark Therapeutics to Participate in Multiple Conferences in February
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Spark Therapeutics (ONCE) Reports Licensing and Supply Agreement for Investigational Voretigene Neparvovec Outside U.S.
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Spark Therapeutics Enters into a Licensing and Supply Agreement for Investigational Voretigene Neparvovec Outside the U.S.
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Spark Therapeutics Enters into a Licensing and Supply Agreement for Investigational Voretigene Neparvovec Outside the U.S.
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Spark Therapeutics Enters into a Licensing and Supply Agreement for Investigational Voretigene Neparvovec Outside the U.S.
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Spark Therapeutics (ONCE) Appoints Robert Perez to Board
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Spark Therapeutics Announces Addition of Robert J. Perez to Board of Directors
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Spark Therapeutics Announces Addition of Robert J. Perez to Board of Directors
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Spark Therapeutics Announces Addition of Robert J. Perez to Board of Directors
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Spark Therapeutics (ONCE) Announces Three New Payer Programs to Improve Patient Access to LUXTURNA (voretigene neparvovec-rzyl)
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Spark Therapeutics Announces First-of-their-kind Programs to Improve Patient Access to LUXTURNA™ (voretigene neparvovec-rzyl), a One-time Gene Therapy Treatment
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Spark Therapeutics Announces First-of-their-kind Programs to Improve Patient Access to LUXTURNA™ (voretigene neparvovec-rzyl), a One-time Gene Therapy Treatment
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Spark Therapeutics to Participate in Multiple Conferences in January
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Spark Therapeutics to Participate in Multiple Conferences in January
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Spark Therapeutics to Participate in Multiple Conferences in January
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FDA Approves Spark Therapeutics' LUXTURNA(TM) (voretigene neparvovec-rzyl), a One-time Gene Therapy for Patients with Confirmed Biallelic RPE65 Mutation-associated Retinal Dystrophy
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Spark Therapeutics (ONCE) Confirms FDA Approval of its LUXTURNA, One-time Gene Therapy for Patients with Confirmed Biallelic RPE65 Mutation-associated Retinal Dystrophy
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FDA Approves Spark Therapeutics’ LUXTURNA™ (voretigene neparvovec-rzyl), a One-time Gene Therapy for Patients with Confirmed Biallelic RPE65 Mutation-associated Retinal Dystrophy
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FDA Approves Spark Therapeutics’ LUXTURNA™ (voretigene neparvovec-rzyl), a One-time Gene Therapy for Patients with Confirmed Biallelic RPE65 Mutation-associated Retinal Dystrophy
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Spark Therapeutics (ONCE) Reports Preliminary Data on Investigational SPK-8011 Phase 1/2 Dose-escalation Clinical Trial in Hemophilia A
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Spark Therapeutics Presents Preliminary Data on Investigational SPK-8011 Phase 1/2 Dose-escalation Clinical Trial in Hemophilia A at 59th American Society of Hematology (ASH) Annual Meeting and Expo
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Spark Therapeutics Presents Preliminary Data on Investigational SPK-8011 Phase 1/2 Dose-escalation Clinical Trial in Hemophilia A at 59th American Society of Hematology (ASH) Annual Meeting and Expo
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Spark Therapeutics (ONCE) and Pfizer (PFE) Announce L-T Prelim. Data Showing Consistent and Sustained Factor IX Levels in Hemophilia B at ASH Meeting
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Spark Therapeutics and Pfizer Announce Longer-term Preliminary Data Showing Consistent and Sustained Factor IX Levels in Hemophilia B at 59th American Society of Hematology (ASH) Annual Meeting and Ex
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Spark Therapeutics and Pfizer Announce Longer-term Preliminary Data Showing Consistent and Sustained Factor IX Levels in Hemophilia B at 59th American Society of Hematology (ASH) Annual Meeting and Ex
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Spark Therapeutics (ONCE), Pfizer (PFE) Announce Publication in NEJM of Interim Data from Phase 1/2 Clinical Trial of Investigational Gene Therapy for Hemophilia B
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Spark Therapeutics and Pfizer Announce Publication in The New England Journal of Medicine of Interim Data from Phase 1/2 Clinical Trial of Investigational Gene Therapy for Hemophilia B
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Spark Therapeutics and Pfizer Announce Publication in The New England Journal of Medicine of Interim Data from Phase 1/2 Clinical Trial of Investigational Gene Therapy for Hemophilia B
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Spark Therapeutics Announces Multiple Presentations on Updated Hemophilia A and Hemophilia B Phase 1/2 Clinical Trials at 59th American Society of Hematology Annual Meeting and Exposition
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Spark Therapeutics (ONCE) Reports Three-Year Follow-up Phase 3 Data Provide Additional Information on Efficacy, Durability and Safety of Investigational LUXTURNA (voretigene neparvovec)
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Three-year Follow-up Phase 3 Data Provide Additional Information on Efficacy, Durability and Safety of Investigational LUXTURNA™ (voretigene neparvovec) in Patients with Biallelic RPE65-mediated Inh
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Spark Therapeutics Reports Third Quarter 2017 Financial Results and Recent Business Progress
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Spark Therapeutics (ONCE), Pfizer (PFE) Amend Pact for Investigational SPK-9001 in Hemophilia B
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Spark Therapeutics and Pfizer Amend License Agreement for Investigational SPK-9001 in Hemophilia B

