Clinical Trials - AGIO

NCT IDTitleStatusPhasesStart DateCompletion DatePrimary Completion Date
NCT06286046A Study of Mitapivat in Participants With Sickle Cell Disease and NephropathyNOT_YET_RECRUITINGPHASE22026-032028-122027-05
NCT07075640A Study to Determine the Safety and Tolerability of AG-236 and How it is Absorbed, Broken Down, and Eliminated From the Body in Healthy ParticipantsRECRUITINGPHASE12025-07-072025-12-122025-10-17
NCT06924970A Dose-Finding Study of Tebapivat to Assess Efficacy, and Safety in Participants With Sickle Cell Disease (SCD)RECRUITINGPHASE22025-05-012027-052026-05
NCT06745271A Study to Determine How Tebapivat is Absorbed, Broken Down, and Removed From the Body and the Extent to Which Tebapivat is Made Available in the Body in Healthy ParticipantsCOMPLETEDPHASE12024-12-202025-02-212025-02-21
NCT06648824Study of How Mitapivat Affects Midazolam Blood Levels in Healthy ParticipantsCOMPLETEDPHASE12024-10-172024-12-032024-12-03
NCT06286033Single and Multiple Ascending Dose Study and Food Effect Study for AG181RECRUITINGPHASE12024-02-202025-10-012025-10-01
NCT05777993A Study to Provide Continued Access to Mitapivat for Participants Who Previously Completed an Agios-Sponsored Mitapivat StudyENROLLING_BY_INVITATIONPHASE42023-07-062029-082029-08
NCT05610657A Pharmacokinetic Study of Mitapivat in Participants With Moderate Hepatic Impairment Compared to Matched Healthy Control Participants With Normal Hepatic FunctionCOMPLETEDPHASE12023-01-102023-07-212023-07-21
NCT05490446A Study of Tebapivat (AG-946) in Participants With Anemia Due to Lower-Risk Myelodysplastic Syndromes (LR-MDS)RECRUITINGPHASE22022-11-072028-112025-11
NCT05144256A Study to Evaluate the Efficacy and Safety of Mitapivat in Pediatric Participants With Pyruvate Kinase Deficiency (PKD) Who Are Regularly Transfused, Followed by a 5-Year Extension PeriodACTIVE_NOT_RECRUITINGPHASE32022-06-082029-062024-05-03
NCT05175105A Study to Evaluate the Efficacy and Safety of Mitapivat in Pediatric Participants With Pyruvate Kinase Deficiency (PKD) Who Are Not Regularly Transfused, Followed by a 5-Year Extension PeriodACTIVE_NOT_RECRUITINGPHASE32022-06-062030-012024-12-13
NCT05031780A Study Evaluating the Efficacy and Safety of Mitapivat (AG-348) in Participants With Sickle Cell Disease (RISE UP)ACTIVE_NOT_RECRUITINGPHASE2, PHASE32022-02-112030-022025-10
NCT04770753A Study Evaluating the Efficacy and Safety of Mitapivat in Participants With Non-Transfusion-Dependent Alpha- or Beta-Thalassemia (α- or β-NTDT)ACTIVE_NOT_RECRUITINGPHASE32021-12-202028-122023-11-13
NCT04770779A Study Evaluating the Efficacy and Safety of Mitapivat in Participants With Transfusion-Dependent Alpha- or Beta-Thalassemia (α- or β-TDT)ACTIVE_NOT_RECRUITINGPHASE32021-11-302029-062024-04-11
NCT04696393A Study to Compare the Pharmacokinetics and Safety of Mitapivat 100 mg Tablet Formulation With Mitapivat 2 × 50 mg Tablet Formulation in Healthy Adult ParticipantsCOMPLETEDPHASE12021-01-062021-03-192021-03-19
NCT04565678A Study to Assess the Relative Bioavailability and Effect of Food on the Coated Granule Formulation of Mitapivat in Healthy ParticipantsCOMPLETEDPHASE12020-09-212020-12-032020-12-03
NCT04536792A Study to Assess the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of AG-946 in Healthy Volunteers and in Participants With Sickle Cell DiseaseCOMPLETEDPHASE12020-07-102023-12-192023-12-19
NCT04472832A Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of Mitapivat (AG-348) in Healthy Adult ParticipantsCOMPLETEDPHASE12020-06-172020-11-232020-11-23
NCT04145128A Study to Evaluate AG-881 in Healthy Japanese and Non-Asian ParticipantsCOMPLETEDPHASE12019-10-022019-12-182019-12-11
NCT04128787A Study to Compare the Relative Bioavailability of Two AG-881 Formulations and Evaluate the Effect of Food and Omeprazole on the Pharmacokinetics of AG-881COMPLETEDPHASE12019-09-302019-12-182019-12-18
NCT04015687A Study to Evaluate the Effect of AG-881 on the Pharmacokinetics of a Single Dose of Lamotrigine in Healthy AdultsCOMPLETEDPHASE12019-07-152019-10-092019-10-09
NCT03991312Study to Evaluate the Effect of Multiple Doses of Itraconazole and Rifampin on the Single-Dose Pharmacokinetics of Mitapivat Sulfate (AG-348) in Healthy Adult ParticipantsCOMPLETEDPHASE12019-06-202019-09-102019-08-14
NCT03834584A Study of AG-636 in the Treatment of Subjects With Advanced LymphomaTERMINATEDPHASE12019-05-242020-06-172020-06-17
NCT03960502A Safety and Pharmacokinetic Study of AG-881 in Healthy Male Participants Following Administration of a Single Oral Dose of [14C] AG-881 and Concomitant Intravenous Microdose of [13C315N3] AG-881COMPLETEDPHASE12019-05-162019-09-072019-09-07
NCT03853798Extension Study of AG-348 in Adult Participants With Pyruvate Kinase Deficiency Previously Enrolled in AG-348-006 or AG348-C-007COMPLETEDPHASE32019-03-212024-07-032024-07-03
NCT03692052A Study to Determine the Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics of AG-348 in Adult Participants With Non-transfusion-dependent ThalassemiaACTIVE_NOT_RECRUITINGPHASE22019-03-202030-09-302020-08-20
NCT03548220A Study to Evaluate Efficacy and Safety of AG-348 in Not Regularly Transfused Adult Participants With Pyruvate Kinase Deficiency (PKD)COMPLETEDPHASE32018-08-092020-10-092020-10-09
NCT03559699A Study Evaluating the Efficacy and Safety of AG-348 in Regularly Transfused Adult Participants With Pyruvate Kinase Deficiency (PKD)COMPLETEDPHASE32018-06-262020-11-122020-11-12
NCT03703505A Study to Evaluate the Absorption, Distribution, Metabolism, Excretion and Absolute Bioavailability of AG-348 in Healthy Male Participants Following Administration of a Single Oral Dose of [14C]AG-348 and Concomitant Single Intravenous Microdose of [13C6]AG-348COMPLETEDPHASE12018-05-242018-06-042018-06-01
NCT03397329Study to Evaluate the Relative Bioavailability and Safety of the AG-348 Tablet and Capsule Formulations in Healthy AdultsCOMPLETEDPHASE12017-10-032017-11-132017-11-13
NCT03282513A Study of AG-120 (Ivosidenib) in Subjects With Mild or Moderate Hepatic Impairment or Normal Hepatic FunctionCOMPLETEDPHASE12017-09-262018-03-312018-03-31
NCT03250598Study to Evaluate the Pharmacokinetics, Safety, and QTc Effect of AG-348 in Healthy Subjects of Japanese Origin and Non-Asian OriginCOMPLETEDPHASE12017-08-092017-10-092017-10-02
NCT03071770Japanese Bridging Study of Ivosidenib (AG-120) in Healthy SubjectsCOMPLETEDPHASE12017-03-312017-09-062017-05-09
NCT02831972Drug-Drug Interaction Study of AG120 in Healthy SubjectsCOMPLETEDPHASE12016-062016-102016-09
NCT02630927A Safety and Tolerability Study of AG-519 in Healthy SubjectsTERMINATEDPHASE12015-122016-122016-12
NCT02579707Food Effect Study of AG120 in Healthy SubjectsCOMPLETEDPHASE12015-102016-062016-02
NCT02492737Study of Orally Administered AG-881 in Patients With Advanced Hematologic Malignancies With an IDH1 and/or IDH2 MutationCOMPLETEDPHASE12015-08-072018-03-212018-03-21
NCT02476916A Study of AG-348 in Adult Participants With Pyruvate Kinase (PK) DeficiencyCOMPLETEDPHASE22015-06-262025-04-022017-05-08
NCT02489513Study to Investigate the Absorption, Metabolism, and Excretion of [14C]-AG-120COMPLETEDPHASE12015-062015-102015-09
NCT02218346Food Effect Study of AG-221 in Healthy Male SubjectsCOMPLETEDPHASE12014-082015-032014-12
NCT02149966A Phase I Study of AG-348 in Healthy VolunteersCOMPLETEDPHASE12014-052014-112014-11
NCT02108106A Phase I Study of AG-348 in Healthy VolunteersCOMPLETEDPHASE12014-032014-082014-08