Recent blog posts
Skye Bioscience Begins Phase 2 Trial of CB1 Inhibitor Nimacimab in Obesity Patients
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Skye Bioscience Begins Phase 2 Trial of CB1 Inhibitor Nimacimab in Obesity Patients
26 August 2024
Skye Bioscience Initiates Phase 2 CBeyond Trial for its Unique CB1 Inhibitor Nimacimab in Obesity Patients.
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Sutro Biopharma Begins Phase 2 REFRαME-L1 Study on Luvelta for Non-Small Cell Lung Cancer Patients
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Sutro Biopharma Begins Phase 2 REFRαME-L1 Study on Luvelta for Non-Small Cell Lung Cancer Patients
26 August 2024
Sutro Biopharma has initiated and is currently enrolling participants for its global Phase 2 trial, REFRαME-L1, which tests luveltamab tazevibulin (luvelta) in NSCLC patients with Folate Receptor-α expression.
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Monopar Gets Approval to Start Phase 1 Trial of New Radiopharmaceutical for Advanced Cancers
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Monopar Gets Approval to Start Phase 1 Trial of New Radiopharmaceutical for Advanced Cancers
26 August 2024
Monopar Therapeutics revealed that it has obtained Human Research Ethics Committee (HREC) approval in Australia to initiate a Phase 1 clinical trial for its innovative radiopharmaceutical MNPR-101-Lu.
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D&D Pharmatech Initiates Phase 2 Trial of DD01 for Obesity-Related MASLD/MASH Treatment
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D&D Pharmatech Initiates Phase 2 Trial of DD01 for Obesity-Related MASLD/MASH Treatment
23 August 2024
D&D Pharmatech begins Phase 2 trial for DD01, a long-lasting dual GLP-1/Glucagon receptor agonist, to assess its safety and efficacy in overweight/obese individuals with MASLD/MASH.
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NPMA Accepts Second NDA for Kelun-Biotech’s SKB264 in EGFR-Mutant NSCLC
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NPMA Accepts Second NDA for Kelun-Biotech’s SKB264 in EGFR-Mutant NSCLC
23 August 2024
Kelun-Biotech’s TROP2-ADC SKB264 (sac-TMT) has had its second NDA accepted by NPMA for locally advanced or metastatic EGFR-mutant NSCLC.
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IGC Pharma Expands Drug Lineup with Potential GLP-1 Agonist IGC-1A for Metabolic Diseases
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IGC Pharma Expands Drug Lineup with Potential GLP-1 Agonist IGC-1A for Metabolic Diseases
23 August 2024
IGC Pharma Broadens Medication Range to Include Metabolic Diseases with IGC-1A, a Possible New GLP-1 Agonist.
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Azitra Announces Patient Screening and Enrollment for Phase 1b ATR-12 Trial in Netherton Syndrome
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Azitra Announces Patient Screening and Enrollment for Phase 1b ATR-12 Trial in Netherton Syndrome
23 August 2024
Azitra Reveals Initial Patient Screening and Enrollment Plans for Phase 1b ATR-12 Trial in Netherton Syndrome.
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Innovo Therapeutics Unveils Breakthrough Phase 2 Data for Post-Thyroidectomy Scar Treatment INV-001
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Innovo Therapeutics Unveils Breakthrough Phase 2 Data for Post-Thyroidectomy Scar Treatment INV-001
23 August 2024
Innovo Therapeutics Inc. Unveils Phase 2 Clinical Data Highlighting the Breakthrough Effectiveness of INV-001 for Post-Thyroidectomy Scar Treatment.
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U.S. Approves RYBREVANT® and LAZCLUZE™ for Initial, Chemotherapy-Free Treatment of Advanced Lung Cancer with EGFR Mutations
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U.S. Approves RYBREVANT® and LAZCLUZE™ for Initial, Chemotherapy-Free Treatment of Advanced Lung Cancer with EGFR Mutations
23 August 2024
The U.S. has approved RYBREVANT® (amivantamab-vmjw) and LAZCLUZE™ (lazertinib) as an initial treatment without chemotherapy for patients with advanced lung cancer and EGFR mutations.
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Sonnet BioTherapeutics Announces Collaboration on Funded Phase 1/2a Trial of SON-1210 with Chemotherapy for Pancreatic Cancer
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Sonnet BioTherapeutics Announces Collaboration on Funded Phase 1/2a Trial of SON-1210 with Chemotherapy for Pancreatic Cancer
22 August 2024
Sonnet BioTherapeutics Signs Clinical Collaboration for Investigator-Led, Funded Phase 1/2a Trial of SON-1210 with Chemotherapy in Pancreatic Cancer.
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China NMPA Approves PADCEV™ for Advanced Urothelial Cancer Treatment
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China NMPA Approves PADCEV™ for Advanced Urothelial Cancer Treatment
22 August 2024
China's NMPA Grants Approval for PADCEV™ (Enfortumab Vedotin) to Treat Advanced or Metastatic Urothelial Cancer.
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TEPKINLY® (Epcoritamab) Approved by European Commission for Treatment of Adult Relapsed/Refractory Follicular Lymphoma
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TEPKINLY® (Epcoritamab) Approved by European Commission for Treatment of Adult Relapsed/Refractory Follicular Lymphoma
22 August 2024
TEPKINLY® (epcoritamab) Gains Another European Commission Nod for Adult Relapsed/Refractory Follicular Lymphoma Treatment.
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