Recent blog posts
Ascendis Pharma Launches YORVIPATH® for Adult Hypoparathyroidism in Germany and Austria
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Ascendis Pharma Launches YORVIPATH® for Adult Hypoparathyroidism in Germany and Austria
11 February 2024
Ascendis Pharma unveils its second TransCon™ offering: YORVIPATH® hits markets in Germany and Austria, targeting chronic hypoparathyroidism in adults.
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FDA Approves NeuroBo Pharmaceuticals' Phase 1 Study of Obesity Drug DA-1726
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FDA Approves NeuroBo Pharmaceuticals' Phase 1 Study of Obesity Drug DA-1726
11 February 2024
NeuroBo Pharmaceuticals has received approval from the FDA for a Phase 1 clinical study of DA-1726, a new drug aimed at managing obesity.
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Halia Therapeutics Revels $30M Series C Funding for Inflammation Treatments
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Halia Therapeutics Revels $30M Series C Funding for Inflammation Treatments
11 February 2024
Halia Therapeutics has unveiled a $30 million Series C funding round to further develop their innovative range of treatments for inflammation.
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Bio-Thera Solutions Initiates Phase 1B/2A Study for BAT6026 Monoclonal Antibody in Eczema Treatment
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Bio-Thera Solutions Initiates Phase 1B/2A Study for BAT6026 Monoclonal Antibody in Eczema Treatment
9 February 2024
Bio-Thera Solutions has launched an early-stage clinical study, specifically Phase 1B/2A, for its novel monoclonal antibody, BAT6026, aimed at OX40 for treating individuals experiencing moderate to intense eczema.
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New Insights: Vabysmo Effectively Treats Retinal Swelling in Retinal Vein Occlusion Patients
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New Insights: Vabysmo Effectively Treats Retinal Swelling in Retinal Vein Occlusion Patients
9 February 2024
Recent findings on Genentech's drug Vabysmo indicate persistent efficacy in reducing retinal swelling and enhancing eyesight for those with Retinal Vein Occlusion.
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First Participant Dosed in RS Oncology's Phase 2 Trial of RSO-021 for Chest Tumor and Lung Metastases
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First Participant Dosed in RS Oncology's Phase 2 Trial of RSO-021 for Chest Tumor and Lung Metastases
9 February 2024
RS Oncology Confirms Initial Participant Receives Dosage in Stage 2 Trial (MITOPE) Examining RSO-021 in Malignant Chest Tumor and Lung Metastases Therapy.
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Sirius Therapeutics Launches Phase One Study for Innovative Anticoagulant to Combat Thromboembolic Conditions
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Sirius Therapeutics Launches Phase One Study for Innovative Anticoagulant to Combat Thromboembolic Conditions
9 February 2024
Sirius Therapeutics has initiated a first-stage clinical study for an advanced, extended-duration Factor XI siRNA anticoagulant, aimed at addressing thromboembolic conditions.
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Takeda and Protagonist Sign Global Deal for Experimental Blood Disorder Drug, Rusfertide
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Takeda and Protagonist Sign Global Deal for Experimental Blood Disorder Drug, Rusfertide
9 February 2024
Takeda Pharmaceuticals and Protagonist Therapeutics have signed a global licensing and partnership deal for the advanced experimental blood disorder medication, Rusfertide.
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Jaguar Gene Therapy's JAG201 Trials Approved by FDA for Autism and Phelan-McDermid Syndrome Treatment
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Jaguar Gene Therapy's JAG201 Trials Approved by FDA for Autism and Phelan-McDermid Syndrome Treatment
9 February 2024
Jaguar Gene Therapy has received the green light from the FDA to initiate trials on JAG201 targeting a specific genetic variant associated with Autism Spectrum Disorder and Phelan-McDermid Syndrome.
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FDA Approves Adaptimmune's Afami-cel Submission for Advanced Synovial Sarcoma with Expedited Review
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FDA Approves Adaptimmune's Afami-cel Submission for Advanced Synovial Sarcoma with Expedited Review
9 February 2024
Adaptimmune Reveals FDA Approval of Afami-cel Submission for Advanced Synovial Sarcoma Treatment with Expedited Review.
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Sandoz Launches Tyruko®, a Unique Biosimilar for Multiple Sclerosis Treatment, in Germany
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Sandoz Launches Tyruko®, a Unique Biosimilar for Multiple Sclerosis Treatment, in Germany
9 February 2024
Sandoz introduces Tyruko® (natalizumab), a first-of-its-kind biosimilar aimed at treating multiple sclerosis, now available in Germany.
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J&J Seeks FDA Approval for DARZALEX FASPRO in Treating Newly Diagnosed Multiple Myeloma Cases
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J&J Seeks FDA Approval for DARZALEX FASPRO in Treating Newly Diagnosed Multiple Myeloma Cases
9 February 2024
Johnson & Johnson has filed an additional request with the FDA for authorization of its DARZALEX FASPRO formula as a therapy option for newly identified multiple myeloma cases eligible for transplant.
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