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Immune-Onc Therapeutics Announces Orphan Drug Designation Granted by US FDA for IO-202 (Anti-LILRB4) for the Treatment of Chronic Myelomonocytic Leukemia (CMML)

Immune-Onc Therapeutics Announces Orphan Drug Designation Granted by US FDA for IO-202 (Anti-LILRB4) for the Treatment of Chronic Myelomonocytic Leukemia (CMML)
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United statesPalo altoTara cooperNational cancer instituteOnc therapeutics incGrace groupDrug administrationCalifornia institute for regenerative medicineLeukemia lymphoma society therapy acceleration programNational institutes of healthEuropean hematology associationOnc therapeuticsOrphan drug designationFast track designationFast trackOrphan drug designations

Immune-Onc Therapeutics Announces Clinical Trial Collaboration to Evaluate IO-108 in a Randomized Global Phase 1b/2 Study for First-Line Treatment of Advanced Liver Cancer

Immune-Onc Therapeutics Announces Clinical Trial Collaboration to Evaluate IO-108 in a Randomized Global Phase 1b/2 Study for First-Line Treatment of Advanced Liver Cancer
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Palo altoUnited statesTara cooperCharlene liaoDrug administrationCalifornia institute for regenerative medicineOnc therapeutics incGrace groupLeukemia lymphoma society therapy acceleration programNational cancer instituteRoche groupNational institutes of healthAmerican association for cancer researchAmerican cancer societyNational comprehensive cancer networkOnc therapeutics

Immune-Onc Therapeutics Announces Clinical Trial Collaboration to Evaluate IO-108 in a Randomized Global Phase 1b/2 Study for First-Line Treatment of Advanced Liver Cancer

Immune-Onc Therapeutics, Inc. ("Immune-Onc"), a private, clinical-stage biopharmaceutical company dedicated to advancing novel therapies in immunology and oncology by targeting myeloid cell inhibitory receptors, today announced a Phase 1b/2 clinical.

United statesPalo altoCharlene liaoLeukemia lymphoma society therapy acceleration programNational cancer instituteAmerican cancer societyCalifornia institute for regenerative medicineNational comprehensive cancer networkDrug administrationNational institutes of healthOnc therapeutics incRoche groupProduct serviceAmerican association for cancer researchRandomized global phaseFirst line treatment

BioInvent to Evaluate BI-1206 in Combination with Rituximab and Calquence

BioInvent to Evaluate BI-1206 in Combination with Rituximab and Calquence
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Cecilia hofvanderMartin welschofBioinvent international ab nasdaq stockholmLeukemia lymphoma society therapy acceleration programBioinvent internationalInvent internationalNasdaq stockholmLymphoma societyTherapy acceleration programSenior director investorRisk management

BioInvent International: BioInvent to Evaluate BI-1206 in Combination with Rituximab and Calquence

BioInvent International: BioInvent to Evaluate BI-1206 in Combination with Rituximab and Calquence
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Stefan klotterCecilia hofvanderMartin welschofBioinvent internationalBioinvent international ab nasdaq stockholmLeukemia lymphoma society therapy acceleration programInvent internationalNasdaq stockholmLymphoma societyTherapy acceleration programSenior director investorRisk managementDie performance strategieAssets sie