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press release

May 5, 2017

Alnylam Pharmaceuticals Announces Sanofi Genzyme Opt-in Decision for Co-Development and Co-Commercialization of Fitusiran in Hemophilia and Rare Bleeding Disorders

- Sanofi Genzyme Elects not to Opt in for ALN AS1 in Acute Hepatic Porphyrias Alnylam Intends to Commercialize ALN AS1 Globally upon Product Approval CAMBRIDGE, Mass. (BUSINESS WIRE) Alnylam Pharmaceuticals, Inc. (Nasdaq:ALNY), the leading RNAi therapeutics company today announced that, pursuant to the companies' global alliance signed in January 2014, Sanofi Genzyme elected ...

press release

May 5, 2017

Alnylam Pharmaceuticals and The Medicines Company Announce Publication of Phase 1 Clinical Data with Inclisiran (ALN- PCSsc) in the New England Journal of Medicine

Interim Results from ORION 1 Phase 2 Study of Inclisiran to be Presented in Late Breaking Clinical Trial Session at the American Heart Association Scientific Sessions on November 15, 2016 CAMBRIDGE, Mass. & PARSIPANY, N.J. (BUSINESS WIRE) Alnylam Pharmaceuticals, Inc. (Nasdaq:ALNY), the leading RNAi therapeutics company, and The Medicines Company (Nasdaq:MDCO), a leading biopharmaceutical development ...

press release

May 5, 2017

Alnylam Reports Positive Initial Clinical Activity Results for Givosiran (ALN-AS1), an Investigational RNAi Therapeutic for the Treatment of Acute Hepatic Porphyrias

- In First Cohort (N=4) of Porphyria Patients with Recurrent Attacks, Givosiran Achieves a 74% Mean Decrease in Annualized Attack Rate Company to Meet with Regulatory Authorities for Potential Phase 3 Start in Late 2017 Management to Discuss New Clinical Data in Webcast Conference Call Tomorrow, Sunday, December 4 at 1:00 p.m. ET CAMBRIDGE, Mass. (BUSINESS WIRE) ...

press release

May 5, 2017

Alnylam Reports Positive Interim Clinical Results for Fitusiran from Ongoing Phase 2 Open Label Extension Study in Patients with Hemophilia A or B without Inhibitors

- Once Monthly, Subcutaneous Fitusiran Achieves Median Annualized Bleeding Rate (ABR) of 1.0, with Median Observation Period of 5.7 Months Fitusiran Generally Well Tolerated with No Thromboembolic Events Alnylam On Track to Initiate Phase 3 Program in Early 2017 Management to Discuss New Clinical Data in Webcast Conference Call Today, Sunday, December 4, at 1:00 p.m. ET CAMBRIDGE, ...

press release

May 5, 2017

Alnylam Pharmaceuticals Reports Third Quarter 2016 Financial Results and Highlights Recent Period Activity

- Advanced RNAi Therapeutics Pipeline with Eight Active Clinical Programs and Multiple Clinical Data Presentations Discontinued Revusiran Development, Focusing on Patisiran and ESC GalNAc Conjugate Programs Company Announces Initiation of Expanded Access Program with Patisiran for Patients with Hereditary ATTR Amyloidosis with Polyneuropathy Maintained Strong Balance Sheet with $1.19 Billion in Cash and Remains On Track to End ...

press release

May 5, 2017

Alnylam to Expand Global Footprint with New European Office in Maidenhead, UK

CAMBRIDGE, Mass. & MAIDENHEAD, United Kingdom (BUSINESS WIRE) Alnylam Pharmaceuticals, Inc. (Nasdaq:ALNY), the leading RNAi therapeutics company, today announced the expansion of its global footprint with the opening of a new development and commercial hub in Maidenhead, UK. In anticipation of substantial growth across Alnylam over the next five years, the office opens with ...

press release

May 5, 2017

Alnylam Presents Clinical and Non-Clinical Data Demonstrating Continued RNAi Platform Optimization and Leadership in the Development of RNA-Based Therapeutics at 12th Annual Meeting of the Oligonucleotide Therapeutics Society

  Clinical Data from Phase 1/2 Study of ALN AAT, an Investigational RNAi Therapeutic Targeting Alpha 1 Antitrypsin (AAT) for the Treatment of AAT Deficiency Associated Liver Disease, Demonstrate Dose Dependent and Durable AAT Knockdown Company to Pursue Follow On Candidate with Improved Tolerability Profile; Expects to File Clinical Trial Application in 2017 In Addition, Alnylam Presents Non Clinical Data ...

press release

May 5, 2017

Data Monitoring Committee Recommends Continuation of APOLLO Phase 3 Clinical Trial of Patisiran for Hereditary ATTR Amyloidosis with Polyneuropathy (hATTR-PN)

- Expected Top line Data Readout Remains Unchanged in Mid 2017 CAMBRIDGE, Mass. (BUSINESS WIRE) Alnylam Pharmaceuticals, Inc. (NASDAQ:ALNY), the leading RNAi therapeutics company, announced today that the Data Monitoring Committee (DMC) for the Phase 3 APOLLO study of patisiran in patients with hereditary ATTR amyloidosis with polyneuropathy (hATTR PN) met on October 7, 2016 ...

press release

May 5, 2017

Alnylam Reports Positive Initial Results from Ongoing Phase 1/2 Study of ALN-GO1, an Investigational RNAi Therapeutic for the Treatment of Primary Hyperoxaluria Type 1

- ALN GO1 Achieves Human Proof of Concept with Statistically Significant Increases in Glycolate, a Biomarker of Effective Glycolate Oxidase Knockdown, in Healthy Adult Volunteers Single Doses of ALN GO1 Found to be Generally Well Tolerated Company to Discuss Clinical Data during ALN GO1 RNAi Roundtable on Tuesday, September 27 at 10:00 a.m. ET CAMBRIDGE, Mass. (BUSINESS WIRE) ...

press release

May 5, 2017

Alnylam Pharmaceuticals Reports Second Quarter 2016 Financial Results and Highlights Recent Period Progress

- Advanced Two Programs into Phase 1 Clinical Studies: ALN TTRsc02 for Transthyretin Mediated Amyloidosis and ALN HBV for Chronic Hepatitis B Virus Infection Presented Clinical Data from Patisiran, Revusiran, Fitusiran, and ALN CC5 Programs Maintained Strong Balance Sheet with $1.28 Billion in Cash and Remains On Track to End 2016 with Greater than $1.0 Billion in Cash CAMBRIDGE, Mass. (BUSINESS ...