Recent blog posts
Eccogene obtains exclusive license from AstraZeneca to develop and sell ECC5004, a GLP-1 receptor agonist for cardio-metabolic diseases
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Eccogene obtains exclusive license from AstraZeneca to develop and sell ECC5004, a GLP-1 receptor agonist for cardio-metabolic diseases
17 November 2023
Eccogene acquires unique licensing rights from AstraZeneca to advance and market ECC5004, a small molecule GLP-1 receptor agonist, for cardiovascular metabolic conditions.
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Allgenesis announces positive early results for its AG-73305 phase 2a Diabetic Macular Edema study at the American Academy of Ophthalmology
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Allgenesis announces positive early results for its AG-73305 phase 2a Diabetic Macular Edema study at the American Academy of Ophthalmology
17 November 2023
Allgenesis reports promising initial safety and effectiveness results for AG-73305 phase 2a trial tackling Diabetic Macular Edema, presented at the American Academy of Ophthalmology.
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Takeda Gets Green Light from U.S. FDA to Market FRUZAQLA™ (fruquintinib) for a Pre-treated Type of Advanced Colon Cancer
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Takeda Gets Green Light from U.S. FDA to Market FRUZAQLA™ (fruquintinib) for a Pre-treated Type of Advanced Colon Cancer
17 November 2023
Takeda has announced FDA approval for its oral drug, FRUZAQLA™ (fruquintinib), designed to treat adults with metastatic colorectal cancer who have previously received chemotherapy, anti-VEGF, and applicable anti-EGFR therapies.
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The EU approves VANFLYTA®, a new FLT3 inhibitor for FLT3-ITD positive AML patients
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The EU approves VANFLYTA®, a new FLT3 inhibitor for FLT3-ITD positive AML patients
17 November 2023
The EU has sanctioned VANFLYTA®, the initial FLT3 inhibitor tailored for recently identified patients with FLT3-ITD positive AML.
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Orum Therapeutics has revealed that Bristol Myers Squibb has taken over its ORM-6151 program
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Orum Therapeutics has revealed that Bristol Myers Squibb has taken over its ORM-6151 program
17 November 2023
Orum Therapeutics has announced a final agreement with Bristol Myers Squibb for the acquisition of its ORM-6151 program.
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BioRay begins Phase I trial for BRY812, a novel LIV-1 antibody drug conjugate, with its first patient
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BioRay begins Phase I trial for BRY812, a novel LIV-1 antibody drug conjugate, with its first patient
17 November 2023
BioRay introduces the initiation of its Phase I clinical trial with the first patient for BRY812, a new LIV-1 focused antibody drug conjugate.
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Ventyx Biosciences announces Phase 2 results for VTX958 in psoriasis and provides a company update
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Ventyx Biosciences announces Phase 2 results for VTX958 in psoriasis and provides a company update
17 November 2023
Ventyx Biosciences reports outcomes of the second phase study of VTX958 in moderate-to-severe plaque psoriasis patients and delivers a company update.
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Monte Rosa Therapeutics reveals preclinical results, suggesting that MRT-6160, could treat immune-based and inflammatory disorders
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Monte Rosa Therapeutics reveals preclinical results, suggesting that MRT-6160, could treat immune-based and inflammatory disorders
16 November 2023
Monte Rosa Therapeutics unveils preclinical findings. The research indicates that MRT-6160, a VAV1-specific molecular glue breaker, may be effective in treating immune-based and inflammatory disorders.
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At SITC 2023, ENB Therapeutics presented early results from phase one of its ENBOLDEN-101 trial for platinum-resistant ovarian cancer
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At SITC 2023, ENB Therapeutics presented early results from phase one of its ENBOLDEN-101 trial for platinum-resistant ovarian cancer
15 November 2023
At SITC 2023, ENB Therapeutics showcased preliminary findings from the first phase of its ENBOLDEN-101 trial for platinum-resistant ovarian cancer.
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Qualigen Therapeutics announces first dose of Phase 1a QN-302 Clinical Study for advanced solid tumors administered to initial patient
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Qualigen Therapeutics announces first dose of Phase 1a QN-302 Clinical Study for advanced solid tumors administered to initial patient
15 November 2023
Qualigen Therapeutics reports the initial dosage in the Phase 1a QN-302 Clinical Study for Advanced or Metastatic Solid Tumors has been administered to the first patient.
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The FDA approves Lilly's Zepbound™ (tirzepatide) - an effective new option for managing continual weight issues such as obesity or health-related overweight conditions
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The FDA approves Lilly's Zepbound™ (tirzepatide) - an effective new option for managing continual weight issues such as obesity or health-related overweight conditions
15 November 2023
The FDA greenlights Lilly's Zepbound™ (tirzepatide) - a potent, new choice for managing persistent weight issues, including obesity or overweight cases with health issues connected to weight.
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ACR 2023: Amgen unveils fresh results from second phase study of dazodalibep for Sjögren's disorder
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ACR 2023: Amgen unveils fresh results from second phase study of dazodalibep for Sjögren's disorder
15 November 2023
Amgen has revealed fresh information from the Phase 2 trial of dazodalibep, an experimental drug aimed to treat Sjögren's.
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