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Merck’s BELSOMRA C-IV meets primary efficacy endpoint in phase 3 trial

May 8, 2019
Merck, known as MSD outside the United States and Canada, announced the presentation of results of a Phase 3 trial evaluating the efficacy and safety of BELSOMRA (suvorexant) C-IV for…
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Bicycle Therapeutics Enters Neuroscience Arena through Collaboration with Dementia Discovery Fund

May 8, 2019
Bicycle Therapeutics, a biotechnology company pioneering a new class of therapeutics based on its proprietary bicyclic peptide (Bicycle) product platform, announced a collaboration with…
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Verve Therapeutics Founded to Protect Against Heart Disease Launches with $58.5 Million in Series A…

May 8, 2019
Verve Therapeutics announced its launch to discover and develop therapies that safely edit the adult human genome to permanently reduce a person’s risk of coronary artery disease, the…
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Dupixent (dupilumab) Approved for Severe Asthma by European Commission

May 8, 2019
The European Commission has approved Dupixent (dupilumab) for use in adults and adolescents 12 years and older as an add-on maintenance treatment for severe asthma with type 2…
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EC Approves LORVIQUA (lorlatinib) for Certain Adult Patients with Previously-Treated ALK-Positive…

May 8, 2019
Pfizer Inc. announced that the European Commission (EC) granted conditional marketing authorization for LORVIQUA (lorlatinib, available in the U.S., Canada and Japan under the brand…
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Sensei Biotherapeutics Announces Clinical Trial Collaboration Agreement with AstraZeneca for Two…

May 7, 2019
Sensei Biotherapeutics, Inc., a clinical-stage biopharmaceutical company developing precision immuno-oncology therapies, announced a clinical trial collaboration with AstraZeneca to…
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Ligand Acquires Milestone and Royalty Rights to SB206 from Novan

May 7, 2019
Ligand Pharmaceuticals Incorporated announces the acquisition of economic rights to SB206 from Novan, Inc. SB206 is a Phase 3 topical antiviral gel for the treatment of skin infections,…
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Xencor Doses First Patient in Phase 1 Study of XmAb23104 for the Treatment of Patients with Advanced…

May 7, 2019
Xencor announced that the first patient has been dosed in XmAb23104-01 (DUET-3), a Phase 1 clinical study to evaluate the safety and tolerability of XmAb23104, a bispecific antibody…
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FDA approves new treatments for heart disease caused by a serious rare disease, transthyretin…

May 7, 2019
On May 3, the U.S. Food and Drug Administration approved Vyndaqel (tafamidis meglumine) and Vyndamax (tafamidis) capsules for the treatment of the heart disease (cardiomyopathy) caused…
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Skyhawk Therapeutics Announces Agreement with Takeda to Develop Novel Small Molecule RNA Splicing…

May 7, 2019
Skyhawk Therapeutics announced a strategic collaboration with Takeda Pharmaceutical Company Limited (Takeda) in which Skyhawk will use its SkySTAR technology platform to discover and…
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Industry Reports

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Press Releases

Industry Leaders Explore the Future of RNA Therapeutics…

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FDA, Health Canada & Leading Biopharma Organizations…

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