Recent blog posts
FDA Clears Full-Life Tech's 225Ac-FL-020 for Treating Metastatic Castration-Resistant Prostate Cancer
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FDA Clears Full-Life Tech's 225Ac-FL-020 for Treating Metastatic Castration-Resistant Prostate Cancer
3 June 2024
Full-Life Technologies Receives FDA IND Clearance for 225Ac-FL-020 to Treat Metastatic Castration-Resistant Prostate Cancer.
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VBI Vaccines Reports New Phase 2b Results for VBI-1901 in Recurrent Glioblastoma
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VBI Vaccines Reports New Phase 2b Results for VBI-1901 in Recurrent Glioblastoma
3 June 2024
VBI Vaccines Releases New Tumor Response Results from Ongoing Phase 2b Study of VBI-1901 in Patients with Recurrent Glioblastoma.
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CDR-Life Begins Phase 1 Trial of CDR404 for Solid Tumors at ASCO
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CDR-Life Begins Phase 1 Trial of CDR404 for Solid Tumors at ASCO
3 June 2024
CDR-Life Inc. has started enrolling participants for the Phase 1 clinical trial of CDR404, their leading candidate being developed as a targeted immunotherapy for the treatment of solid tumors.
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LIB Therapeutics Reveals Positive Phase 3 Lerodalcibep Data at EAS Congress
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LIB Therapeutics Reveals Positive Phase 3 Lerodalcibep Data at EAS Congress
3 June 2024
LIB Therapeutics Shares Positive Phase 3 Lerodalcibep Results at 92nd European Atherosclerosis Society Congress.
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Atara Biotherapeutics Presents Early CAR T Therapy Research on CD19 at ISCT 2024
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Atara Biotherapeutics Presents Early CAR T Therapy Research on CD19 at ISCT 2024
3 June 2024
Atara Biotherapeutics Presents Early Research on ATA3219, a CAR T Therapy Targeting CD19 for B-Cell Autoimmune Diseases, at ISCT 2024.
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Bio-Thera and STADA Sign Exclusive Deal for Golimumab Biosimilar in Europe and UK
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Bio-Thera and STADA Sign Exclusive Deal for Golimumab Biosimilar in Europe and UK
3 June 2024
The partnership involves the commercialization and licensing of BAT2506, a biosimilar of Simponi® (golimumab).
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Outlook Therapeutics Gains EU Approval for Wet AMD Drug LYTENAVA™
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Outlook Therapeutics Gains EU Approval for Wet AMD Drug LYTENAVA™
31 May 2024
Outlook Therapeutics® Gains European Commission Approval for Marketing LYTENAVA™ (bevacizumab gamma) to Treat Wet AMD.
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FDA Grants Approval for First Interchangeable Biosimilar to Treat Two Uncommon Conditions
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FDA Grants Approval for First Interchangeable Biosimilar to Treat Two Uncommon Conditions
31 May 2024
The U.S. Food and Drug Administration has granted approval to Bkemv (eculizumab-aeeb) as the first interchangeable biosimilar to Soliris (eculizumab) for the treatment of specific rare conditions.
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TROPION-Lung01 Trial: Datopotamab Deruxtecan Improves Survival in Advanced Non-Small Cell Lung Cancer
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TROPION-Lung01 Trial: Datopotamab Deruxtecan Improves Survival in Advanced Non-Small Cell Lung Cancer
31 May 2024
In the TROPION-Lung01 Phase III trial, datopotamab deruxtecan significantly improved overall survival compared to chemotherapy in patients with advanced nonsquamous non-small cell lung cancer.
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FDA Grants Priority Review to Sarclisa for Newly Diagnosed Multiple Myeloma Patients Ineligible for Transplant
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FDA Grants Priority Review to Sarclisa for Newly Diagnosed Multiple Myeloma Patients Ineligible for Transplant
31 May 2024
Sarclisa received FDA priority review for treating newly diagnosed multiple myeloma patients ineligible for transplant.
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TILT Biotherapeutics Shares Clinical Results of TILT-123 for Ovarian Cancer at ASCO 2024
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TILT Biotherapeutics Shares Clinical Results of TILT-123 for Ovarian Cancer at ASCO 2024
30 May 2024
TILT Biotherapeutics' one abstract highlights encouraging safety and efficacy findings of TILT-123 in patients with ovarian cancer.
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selectION Announces Phase 1b Trial Start for si-544 in Psoriasis Vulgaris and Psoriatic Arthritis Patients
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selectION Announces Phase 1b Trial Start for si-544 in Psoriasis Vulgaris and Psoriatic Arthritis Patients
30 May 2024
selectION, Inc. declared the commencement of a Phase 1b study involving its leading candidate si-544 in adult individuals suffering from psoriasis vulgaris or psoriatic arthritis.
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