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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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Third Novartis Phase III trial shows Kisqali combination therapy significantly improves PFS in…

Jun 4, 2018
Novartis announced positive results from the third Phase III trial of Kisqali (ribociclib) in advanced or metastatic breast cancer. MONALEESA-3 showed Kisqali plus fulvestrant…
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Press Releases

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