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HUTCHMED Highlights Sovleplenib Phase III ESLIM-01 Study and Hematological Malignancy Programs Data to be Presented at the upcoming EHA2024 Congress

HONG KONG, SHANGHAI and FLORHAM PARK, N.J., May 17, 2024 HUTCHMED Limited today announces that topline and subgroup results from the ESLIM-01 Phase III study of sovleplenib, as well as new.

Ying qianCheng meiHong kongUnited statesRenchi yangPau montesinosZhou yiAtholl tweedieMingci caiHall malloXiaojun huangFengkui zhangXiaofan liuBen atwell alex shawWaleed ghanimaTongji medical college

Kineta (KA) Reports Q1, Provides Update on Phase 1/2 VISTA-101 Trial

Kineta (KA) Reports Q1, Provides Update on Phase 1/2 VISTA-101 Trial
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United statesCraig philipsDartmouth giesel school of medicineAmerican association for cancer researchKineta incSolid cancer tumorsDose escalationTherapy dose escalationHummingbird bioscienceDartmouth giesel schoolKeystone symposiaBeyond immune checkpoint blockadeAmerican associationCancer researchBlood cancer discoveryQuarterly report

Hydroxyurea Dose Escalation Effective for Children with Sickle Cell Anemia

Extended follow-up of a phase 1/2 trial finds hydroxyurea dose optimization significantly improves clinical responses in children in sub-Saharan Africa with sickle cell.

Banu aygunLinkedin banu aygunJulie kanterDrug administrationBirmingham school of medicineCohen children medical centerUniversity of alabamaSaharan africaCohen childrenBirmingham schoolDose escalationSickle cell anemia

Kineta Reports Initial Clinical Response Data at AACR 2024 of its Ongoing Phase 1/2 VISTA-101 Clinical Trial

Kineta Reports Initial Clinical Response Data at AACR 2024 of its Ongoing Phase 1/2 VISTA-101 Clinical Trial
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United statesSan diegoThierry guillaudeuxMerck co incAmerican association for cancer researchMerck sharp dohmeKineta incAmerican associationCancer researchDose escalationTherapy dose escalationChief scientific officerMerck sharpStatements regarding forward lookingPrivate securities litigation reform actAnnual report

Medicenna Presents Updated Results of Single Agent MDNA11 Anti-tumor Activity from Dose Escalation and Ongoing Dose Expansion of the Phase 1/2 ABILITY-1 Study at the 2024 Annual Meeting of the American Association for Cancer Research (AACR)

Medicenna Presents Updated Results of Single Agent MDNA11 Anti-tumor Activity from Dose Escalation and Ongoing Dose Expansion of the Phase 1/2 ABILITY-1 Study at the 2024 Annual Meeting of the American Association for Cancer Research (AACR)
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San diegoUnited statesSuperkine immunotherapiesChristina cameronMerck co incMedicenna therapeutics corpMerck sharp dohmePresents updated resultsSingle agentDose escalationOngoing dose expansionAmerican associationCancer researchFahar merchantChief executive officerRecommended dose