Recent blog posts
Longhorn Vaccine and Diagnostics' data shows lhnvd-201 can neutralize covid-19 and influenza coinfection
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Longhorn Vaccine and Diagnostics' data shows lhnvd-201 can neutralize covid-19 and influenza coinfection
1 October 2023
Data provided by Longhorn vaccine and diagnostics indicate that lhnvd-201 has neutralizing activity against covid-19 and influenza coinfection.
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FDA Grants Approval for Likmez (metronidazole) Liquid Form to Treat Parasitic and Anaerobic Bacteria-Related Conditions
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FDA Grants Approval for Likmez (metronidazole) Liquid Form to Treat Parasitic and Anaerobic Bacteria-Related Conditions
30 September 2023
Appili Therapeutics a biodefense and infectious disease drug company, announced that its production and marketing partner, Saptalis Pharmaceuticals, received US FDA approval for Metronidazole Oral Suspension 500mg/5mL.
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Nova Therapeutics confirms FDA approval of VNT-101's IND application, a new direct-acting antivirus targeting Influenza A virus
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Nova Therapeutics confirms FDA approval of VNT-101's IND application, a new direct-acting antivirus targeting Influenza A virus
30 September 2023
Nova Therapeutics, a biotech firm specializing in Influenza A treatments, received US FDA approval for its IND application for influenza A suppressant, VNT-101.
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Merck's phase III KEYNOTE-A39/EV-302 trial halted disease progression in some new urothelial cancer patients
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Merck's phase III KEYNOTE-A39/EV-302 trial halted disease progression in some new urothelial cancer patients
30 September 2023
Merck reported that the phase III KEYNOTE-A39/EV-302 test halted disease progression in certain patients with local or metastatic urothelial cancer who hadn't received prior treatment.
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Genmab announces EU approval for TEPKINLY® (epcoritamab) to treat adult R/R DLBCL
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Genmab announces EU approval for TEPKINLY® (epcoritamab) to treat adult R/R DLBCL
30 September 2023
Genmab Unveils EU Commission's Authorization for TEPKINLY® (epcoritamab) to Treat Relapsed or Refractory (R/R) Diffuse Large B-cell Lymphoma (DLBCL) in Adults.
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Lutathera®, a Novartis radioligand therapy, significantly improved progression-free survival rates in early advanced GEP-NETs
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Lutathera®, a Novartis radioligand therapy, significantly improved progression-free survival rates in early advanced GEP-NETs
30 September 2023
Lutathera®, a radioligand therapy by Novartis, showed significant progression-free survival rates in initial stage advanced gastroenteropancreatic neuroendocrine tumors (GEP-NETs).
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Henlius' Innovative Anti-PD-1 mAb HANSIZHUANG (Serplulimab) Receives Approval for Use in Treating ESCC
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Henlius' Innovative Anti-PD-1 mAb HANSIZHUANG (Serplulimab) Receives Approval for Use in Treating ESCC
30 September 2023
Shanghai Henlius Biotech, Inc. has made a public announcement that the NMPA has given approval to the NDA for an innovative fresh indication of HANSIZHUANG (serplulimab injection).
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SELLAS announces promising initial results from the SLS009 Phase 1 lymphoma group study, advancing to Phase 2 clinical trial
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SELLAS announces promising initial results from the SLS009 Phase 1 lymphoma group study, advancing to Phase 2 clinical trial
30 September 2023
SELLAS reveals uplifting preliminary findings in Lymphoma group from SLS009 Phase 1 Increasing-Dose Study, promoting progression to Phase 2 Clinical Experiment.
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Krystal Biotech reports FDA approval of the investigational new drug application for KB408 to treat Type 1 Alpha-1 Antitrypsin Deficiency
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Krystal Biotech reports FDA approval of the investigational new drug application for KB408 to treat Type 1 Alpha-1 Antitrypsin Deficiency
30 September 2023
Krystal Biotech publicized that the U.S. FDA has given the green light for the Investigational New Drug application for KB408 to manage alpha-1 antitrypsin deficiency.
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The European Commission has approved Jazz Pharmaceuticals' Enrylaze® for Acute Lymphoblastic Leukemia and Lymphoblastic Lymphoma treatment
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The European Commission has approved Jazz Pharmaceuticals' Enrylaze® for Acute Lymphoblastic Leukemia and Lymphoblastic Lymphoma treatment
30 September 2023
Jazz Pharmaceuticals plc has proclaimed that the EC has approved the commercialization of Enrylaze®(JZP458; a derivative of Erwinia asparaginase or crisantaspase).
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Leucid Bio receives MHRA approval to clinically test LEU011, a Lateral NKG2D CAR-T Cell treatment
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Leucid Bio receives MHRA approval to clinically test LEU011, a Lateral NKG2D CAR-T Cell treatment
30 September 2023
Leucid Bio announced today its UK MHRA-approved CTA to commence Phase 1/2 AERIAL clinical trials of its drug, LEU011, for treating adult patients with relapsed or resistant solid tumours.
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BMS reports improved survival in operable non-small cell lung cancer patients with a regimen of Opdivo (nivolumab) and chemotherapy
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BMS reports improved survival in operable non-small cell lung cancer patients with a regimen of Opdivo (nivolumab) and chemotherapy
28 September 2023
Bristol Myers Squibb states that a pre/postoperative regimen of Opdivo (nivolumab) and chemotherapy significantly improves survival in operable non-small cell lung cancer patients.
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