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BlackThorn Therapeutics Initiates Phase 1 Study of BTRX-335140, an Investigational Kappa Opioid…

Jun 7, 2018
BlackThorn Therapeutics announced enrollment of the first healthy volunteers in a Phase 1 study of BTRX-335140, a kappa opioid receptor (KOR) antagonist that targets brain circuits that…
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Chugai’s HEMLIBRA Receives Priority Review Status from FDA for Hemophilia A Without Inhibitors

Jun 6, 2018
Chugai Pharmaceutical announced that the U.S. Food and Drugs Administration (FDA) has accepted the supplemental Biologics License Application (sBLA) and granted Priority Review for…
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Hookipa and Gilead Enter into a Collaboration and License Agreement to Develop Immunotherapies…

Jun 6, 2018
Hookipa Biotech AG and Gilead Science announced that they have entered into a research collaboration and license agreement that grants Gilead exclusive rights to Hookipa’s TheraT and…
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InflaRx Opens New Research Facility in Ann Arbor

Jun 6, 2018
InflaRx, a biopharmaceutical company developing innovative therapeutics to treat life-threatening inflammatory diseases by targeting the complement system, a key component of the innate…
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Sensei Biotherapeutics Reports New Data from Phase 1 Clinical Trial of SNS-301

Jun 6, 2018
Sensei Biotherapeutics announced the publication of data from the company’s multi-center Phase 1 clinical trial to assess safety and immunogenicity of SNS-301 (formerly PAN-301) in…
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Internationally Recognised Biobanks Sign Up To 8th Annual BioBanking Conference

Jun 5, 2018
SMi Reports: Internationally recognized biobanks sign up for 8th annual BioBanking conference, taking place in just 1 week in London. With just a week left until the 8th Annual…
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Virpax Pharmaceuticals Licenses Liposome Drug Delivery Technology From LipoCure

Jun 5, 2018
Virpax Pharmaceuticals signed a technology license agreement with LipoCure to develop pain management products using its liposome drug delivery technology. The first investigational…
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FDA Approves Mylan and Biocon’s Fulphila (pegfilgrastim-jmdb), the First Biosimilar to…

Jun 5, 2018
Mylan and Biocon announced that the U.S. Food and Drug Administration (FDA) has approved Mylan's Fulphila (pegfilgrastim-jmbd), a biosimilar to Neulasta (pegfilgrastim), co-developed…
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Official programme released for SMi’s 8th annual Orphan Drugs and Rare Diseases conference

Jun 4, 2018
SMi Group reports: fresh off the press - official agenda for Orphan Drugs and Rare Diseases taking place on 17 - 18 October in London   Patients with rare diseases cannot continue to…
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Merck’s KEYTRUDA (pembrolizumab) Showed Overall Response Rate of Nearly 40 Percent as First-Line…

Jun 4, 2018
Merck announced interim results from Cohort A of KEYNOTE-427, a Phase 2 trial evaluating KEYTRUDA, Merck’s anti-PD-1 therapy, as first-line treatment for advanced clear cell renal cell…
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