Pharmaceutical Insights
Navigate pharmaceutical trends with our insights on targets, institutional pipelines, clinical advances, and new drugs.
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Recent blog posts
Boehringer gains U.S. FDA Breakthrough Therapy status and starts two phase III MASH trials for survodutide
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Boehringer gains U.S. FDA Breakthrough Therapy status and starts two phase III MASH trials for survodutide
11 October 2024
Boehringer Ingelheim has revealed that survodutide (BI 456906) has received the Breakthrough Therapy designation from the U.S. Food and Drug Administration (FDA).
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First Dosing of Halia Therapeutics' Oral LRRK2 Inhibitor HT-4253 in Alzheimer's Study
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First Dosing of Halia Therapeutics' Oral LRRK2 Inhibitor HT-4253 in Alzheimer's Study
11 October 2024
Halia Therapeutics revealed the initial dosing of HT-4253, an innovative oral LRRK2 inhibitor aimed at reducing neuroinflammation in Alzheimer's, in a healthy participant.
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MediLink Reveals Worldwide Partnership and Supply Deal for YL201 Combo Treatment
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MediLink Reveals Worldwide Partnership and Supply Deal for YL201 Combo Treatment
11 October 2024
MediLink Therapeutics announced a partnership for a global clinical trial and a supply agreement with Amgen Inc. Under this agreement.
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Pharma Frontiers: Daily Digest of Global Pharmaceutical News – Oct 10
Pharma Frontiers: Daily Digest of Global Pharmaceutical News – Oct 10
11 October 2024
Oct 10th latest updates in the global new drug development field, including progress in new drug research and development, transaction information, and partnership developments.
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TiumBio Reports Initial Patient Dosing in Phase 2 Trial for TU2218, an Oral Immuno-Oncology Medication
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TiumBio Reports Initial Patient Dosing in Phase 2 Trial for TU2218, an Oral Immuno-Oncology Medication
9 October 2024
TiumBio announced that it has administered the first dose to a patient in its Phase 2 clinical study of TU2218.
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Pharma Frontiers: Daily Digest of Global Pharmaceutical News – Oct 9
Pharma Frontiers: Daily Digest of Global Pharmaceutical News – Oct 9
9 October 2024
Oct 9th latest updates in the global new drug development field, including progress in new drug research and development, transaction information, and partnership developments.
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Kezar Life Sciences Reports Clinical Hold on Zetomipzomib IND for Lupus Nephritis Treatment
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Kezar Life Sciences Reports Clinical Hold on Zetomipzomib IND for Lupus Nephritis Treatment
9 October 2024
Kezar Life Sciences were informed that the IND application for zetomipzomib, intended for lupus nephritis (LN) treatment, has been put on clinical hold.
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Eton Pharmaceuticals, Inc plans to purchase Increlex® (mecasermin injection) from Ipsen
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Eton Pharmaceuticals, Inc plans to purchase Increlex® (mecasermin injection) from Ipsen
9 October 2024
Eton Pharmaceuticals revealed that it has engaged in an asset purchase deal to obtain Increlex® (mecasermin injection) from Ipsen S.A.
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Theriva™ Biologics Announces Positive Review by Data and Safety Committee in Early Stage Trial of SYN-004 for Transplant Patients
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Theriva™ Biologics Announces Positive Review by Data and Safety Committee in Early Stage Trial of SYN-004 for Transplant Patients
9 October 2024
Theriva™ Biologics Reports Favorable Results in Phase 1b/2a Trial of SYN-004 (ribaxamase) for Allogeneic Hematopoietic Cell Transplant Patients.
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ABL Bio to Collaborate on Testing ABL103 with KEYTRUDA® (pembrolizumab) for Solid Tumor Patients
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ABL Bio to Collaborate on Testing ABL103 with KEYTRUDA® (pembrolizumab) for Solid Tumor Patients
9 October 2024
ABL Bio, revealed that it has formed a clinical trial collaboration and supply agreement with MSD.
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Alentis Therapeutics Secures FDA IND Approval for Innovative CLDN1-ADC, ALE.P02
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Alentis Therapeutics Secures FDA IND Approval for Innovative CLDN1-ADC, ALE.P02
9 October 2024
Alentis Therapeutics gains FDA IND approval for ALE.P02, an innovative CLDN1-ADC targeting the treatment of squamous cell cancers.
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FDA Approves Opdivo® with Chemotherapy for Pre- and Post-Surgery Treatment in Resectable NSCLC
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FDA Approves Opdivo® with Chemotherapy for Pre- and Post-Surgery Treatment in Resectable NSCLC
9 October 2024
The FDA has authorized the use of Opdivo® (nivolumab) with chemotherapy before surgery and as a post-surgery treatment for resectable NSCLC.
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