Clinical Trials Directory

Trials / Sponsors / Agios Pharmaceuticals, Inc.

Agios Pharmaceuticals, Inc.

Industry · 50 registered clinical trials6 currently recruiting.

StatusTrialPhaseStarted
Not Yet RecruitingA Study to Investigate the Efficacy, Pharmacokinetics, and Safety of Mitapivat in Pediatric Participants With
Non-Transfusion-dependent Alpha-Thalassemia, Non-Transfusion-dependent Beta-Thalassemia
Phase 32026-09-01
Not Yet RecruitingA Study to Investigate the Efficacy, Pharmacokinetics, and Safety of Mitapivat in Pediatric Participants With
Transfusion-dependent Alpha-Thalassemia, Transfusion-dependent Beta-Thalassemia
Phase 32026-09-01
Not Yet RecruitingA Study to Evaluate Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of AG-181 in Subjects With Ph
Phenylketonuria
Phase 12026-03-01
WithdrawnA Study of Mitapivat in Participants With Sickle Cell Disease and Nephropathy
Sickle Cell Disease, Nephropathy
Phase 22026-03-01
RecruitingA Study to Determine the Safety and Tolerability of AG-236 and How it is Absorbed, Broken Down, and Eliminated
Healthy Participants
Phase 12025-07-07
RecruitingA Dose-Finding Study of Tebapivat to Assess Efficacy, and Safety in Participants With Sickle Cell Disease (SCD
Sickle Cell Disease
Phase 22025-05-01
CompletedA Study to Determine How Tebapivat is Absorbed, Broken Down, and Removed From the Body and the Extent to Which
Healthy Participants
Phase 12024-12-20
CompletedStudy of How Mitapivat Affects Midazolam Blood Levels in Healthy Participants
Healthy Participants
Phase 12024-10-17
CompletedSingle and Multiple Ascending Dose Study and Food Effect Study for AG181
Healthy Volunteers
Phase 12024-02-20
Enrolling By InvitationA Study to Provide Continued Access to Mitapivat for Participants Who Previously Completed an Agios-Sponsored
Pyruvate Kinase Deficiency, Anemia, Hemolytic
Phase 42023-07-06
CompletedA Pharmacokinetic Study of Mitapivat in Participants With Moderate Hepatic Impairment Compared to Matched Heal
Moderate Hepatic Impairment
Phase 12023-01-10
Active Not RecruitingA Study of Tebapivat (AG-946) in Participants With Anemia Due to Lower-Risk Myelodysplastic Syndromes (LR-MDS)
Myelodysplastic Syndromes
Phase 22022-11-07
Active Not RecruitingA Study to Evaluate the Efficacy and Safety of Mitapivat in Pediatric Participants With Pyruvate Kinase Defici
Pediatric Pyruvate Kinase Deficiency, Pediatric Hemolytic Anemia
Phase 32022-06-08
Active Not RecruitingA Study to Evaluate the Efficacy and Safety of Mitapivat in Pediatric Participants With Pyruvate Kinase Defici
Pediatric Pyruvate Kinase Deficiency, Pediatric Hemolytic Anemia
Phase 32022-06-06
Active Not RecruitingA Study Evaluating the Efficacy and Safety of Mitapivat (AG-348) in Participants With Sickle Cell Disease (RIS
Sickle Cell Disease
Phase 2 / Phase 32022-02-11
Active Not RecruitingA Study Evaluating the Efficacy and Safety of Mitapivat in Participants With Non-Transfusion-Dependent Alpha-
Non-Transfusion-dependent Alpha-Thalassemia, Non-Transfusion-dependent Beta-Thalassemia
Phase 32021-12-20
Active Not RecruitingA Study Evaluating the Efficacy and Safety of Mitapivat in Participants With Transfusion-Dependent Alpha- or B
Transfusion-dependent Alpha-Thalassemia, Transfusion-dependent Beta-Thalassemia
Phase 32021-11-30
TerminatedPyruvate Kinase (PK) Deficiency Global Longitudinal Registry: Patient-Reported Outcomes (PRO)
Pyruvate Kinase Deficiency, Pyruvate Kinase Deficiency Anemia, Anemia
2021-07-02
CompletedPyruvate Kinase Deficiency Global Longitudinal Registry Substudy of Protocol AG348-C-008
Pyruvate Kinase Deficiency
2021-07-02
CompletedA Study to Compare the Pharmacokinetics and Safety of Mitapivat 100 mg Tablet Formulation With Mitapivat 2 × 5
Healthy Volunteers
Phase 12021-01-06
CompletedA Study to Assess the Relative Bioavailability and Effect of Food on the Coated Granule Formulation of Mitapiv
Healthy Volunteers
Phase 12020-09-21
CompletedA Study to Assess the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of AG-946 in Healthy Volunt
Healthy Volunteers, Anemia, Sickle Cell
Phase 12020-07-10
CompletedA Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of Mitapivat (AG-348) in Healthy Adult Part
Healthy Volunteers
Phase 12020-06-17
CompletedA Study to Evaluate AG-881 in Healthy Japanese and Non-Asian Participants
Healthy Volunteers
Phase 12019-10-02
CompletedA Study to Compare the Relative Bioavailability of Two AG-881 Formulations and Evaluate the Effect of Food and
Healthy Volunteers
Phase 12019-09-30
CompletedA Study to Evaluate the Effect of AG-881 on the Pharmacokinetics of a Single Dose of Lamotrigine in Healthy Ad
Healthy Participants
Phase 12019-07-15
CompletedStudy to Evaluate the Effect of Multiple Doses of Itraconazole and Rifampin on the Single-Dose Pharmacokinetic
Healthy Volunteers
Phase 12019-06-20
TerminatedA Study of AG-636 in the Treatment of Subjects With Advanced Lymphoma
Lymphoma
Phase 12019-05-24
CompletedA Safety and Pharmacokinetic Study of AG-881 in Healthy Male Participants Following Administration of a Single
Healthy Male Participants
Phase 12019-05-16
CompletedExtension Study of AG-348 in Adult Participants With Pyruvate Kinase Deficiency Previously Enrolled in AG-348-
Pyruvate Kinase Deficiency
Phase 32019-03-21
Active Not RecruitingA Study to Determine the Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics of AG-348 in Adult Participa
Thalassemia
Phase 22019-03-20
CompletedA Study to Evaluate Efficacy and Safety of AG-348 in Not Regularly Transfused Adult Participants With Pyruvate
Pyruvate Kinase Deficiency, Anemia, Hemolytic
Phase 32018-08-09
CompletedA Study Evaluating the Efficacy and Safety of AG-348 in Regularly Transfused Adult Participants With Pyruvate
Pyruvate Kinase Deficiency, Anemia, Hemolytic
Phase 32018-06-26
CompletedA Study to Evaluate the Absorption, Distribution, Metabolism, Excretion and Absolute Bioavailability of AG-348
Healthy Volunteers
Phase 12018-05-24
Active Not RecruitingPyruvate Kinase Deficiency Global Longitudinal Registry
Pyruvate Kinase Deficiency
2018-04-23
CompletedPre-Screening Study to Identify MTAP Loss in Advanced Solid Tumors or Lymphoma
Advanced Solid Tumors, Lymphoma
2018-03-01
CompletedStudy to Evaluate the Relative Bioavailability and Safety of the AG-348 Tablet and Capsule Formulations in Hea
Healthy Volunteers
Phase 12017-10-03
CompletedA Study of AG-120 (Ivosidenib) in Subjects With Mild or Moderate Hepatic Impairment or Normal Hepatic Function
Hepatic Impairment
Phase 12017-09-26
CompletedStudy to Evaluate the Pharmacokinetics, Safety, and QTc Effect of AG-348 in Healthy Subjects of Japanese Origi
Healthy, Japanese, Non-Asian
Phase 12017-08-09
CompletedJapanese Bridging Study of Ivosidenib (AG-120) in Healthy Subjects
Healthy
Phase 12017-03-31
CompletedDrug-Drug Interaction Study of AG120 in Healthy Subjects
Healthy
Phase 12016-06-01
TerminatedA Safety and Tolerability Study of AG-519 in Healthy Subjects
Anemia
Phase 12015-12-01
CompletedFood Effect Study of AG120 in Healthy Subjects
Healthy
Phase 12015-10-01
CompletedStudy of Orally Administered AG-881 in Patients With Advanced Hematologic Malignancies With an IDH1 and/or IDH
Acute Myeloid Leukemia (AML), Myelodysplastic Syndrome, Hematologic Malignancies
Phase 12015-08-07
CompletedA Study of AG-348 in Adult Participants With Pyruvate Kinase (PK) Deficiency
Pyruvate Kinase Deficiency
Phase 22015-06-26
CompletedStudy to Investigate the Absorption, Metabolism, and Excretion of [14C]-AG-120
Healthy Volunteers
Phase 12015-06-01
CompletedFood Effect Study of AG-221 in Healthy Male Subjects
Healthy Volunteers
Phase 12014-08-01
CompletedA Phase I Study of AG-348 in Healthy Volunteers
Healthy Volunteer
Phase 12014-05-01
CompletedA Phase I Study of AG-348 in Healthy Volunteers
Healthy Volunteer
Phase 12014-03-01
Approved For MarketingIvosidenib Expanded Access Program in Relapsed/Refractory AML With an IDH1 Mutation
Acute Myeloid Leukemia, Relapsed Adult AML, Relapsed Pediatric AML