TheraRadar
Data updated: May 26, 2026

ASTAGRAF XL (tacrolimus)

Genetic Support
Immunology Approved 2013-07-19

Astagraf XL helps prevent the body from rejecting a new organ in patients who have undergone a kidney transplant. It is used for both adults and children who are able to swallow the capsules intact. This medication is typically prescribed in combination with other immunosuppressive drugs to support the long-term health of the transplant.

Source: FDA Label • ASTELLAS

How ASTAGRAF XL Works

This medication works by binding to the intracellular protein FKBP-12 to form a complex that inhibits calcineurin, an enzyme essential for immune cell signaling. This process blocks the production of several inflammatory cytokines and prevents the activation and growth of T-lymphocytes. By suppressing these specific immune responses, the drug helps protect the transplanted organ from being attacked by the patient's immune system.

2
Indications
--
Phase 3 Trials
12
Years on Market

Details

Status
Prescription
First Approved
2013-07-19
Routes
ORAL
Dosage Forms
CAPSULE, EXTENDED RELEASE

Companies

Active Ingredient: TACROLIMUS

ASTAGRAF XL Approval History

2014
2015
2016
2017
2018
2019
2020
2021
2022
2023
2024
2025
2026
Original
New Indication
New Form
Label Update
30 FDA actions from 2013 to 2023 · 1 indication expansions
Sep 2023 SUPPL
Label · Labeling
Nov 2022 SUPPL
Label · Labeling
Dec 2020 SUPPL
Label · Labeling

What ASTAGRAF XL Treats

1 indications

ASTAGRAF XL is approved for 1 conditions since its original approval in 2013. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Organ Rejection
Source: FDA Label

ASTAGRAF XL Boxed Warning

MALIGNANCIES AND SERIOUS INFECTIONS IN TRANSPLANT PATIENTS; AND INCREASED MORTALITY IN FEMALE LIVER TRANSPLANT PATIENTS • Increased risk for developing serious infections and malignancies with ASTAGRAF XL ® or other immunosuppressants that may lead to hospitalization or death. [see Warnings and Precautions ( 5.1 , 5.2 )] • Increased mortality in female liver transplant patients with ASTAGRAF XL. ASTAGRAF XL is not approved for use in liver transplantation. [see Warnings and Precautions ( 5.3 )] ...

ASTAGRAF XL Target & Pathway

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Target

IL-2 (Interleukin 2) Cytokine

ASTAGRAF XL Competitive Set

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Filters applied: drops same-active-ingredient (505(b)(2) reformulations), route-mismatch (topical vs systemic), and cross-therapeutic-area matches in same-indication rings.

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Clinical Trial Registry

371 trials
Trial Sponsor ID Phase Status Title
NCT07524530 10002233 002233-C Ph 2 not yet recruiting Stem Cell Transplantation for Participants With Germline RUNX1 Associated Blood Cancers
NCT05088356 IRB-60439 NCI-2021-12228 Ph 1 active not recruiting Reduced Intensity Allogeneic HCT in Advanced Hematologic Malignancies w/T-Cell Depleted Graft
NCT07582172 25663 NCI-2026-03208, 25663 Ph 2 not yet recruiting Total Marrow and Lymphoid Irradiation in Combination With Fludarabine and Melphalan as Conditioning for Allogeneic Peripheral Blood Stem Cell Hematopoietic Cell Transplant in Older Patients With Refractory and Relapsed Acute Myeloid Leukemia and High-risk Myelodysplastic Syndrome
NCT07204275 OLYMPUS VX24-AIS-D10 2025-521661-27-00 Ph 2, Ph 3 recruiting Evaluation of Efficacy, Safety, and Tolerability of Povetacicept in Participants With Primary Membranous Nephropathy (pMN)
NCT06996119 23822 NCI-2025-03603, 23822 Ph 1 recruiting Emapalumab With Post-Transplant Cyclophosphamide, Tacrolimus and Mycophenolate Mofetil for the Prevention of Graft-versus-Host Disease After Donor Reduced-Intensity Hematopoietic Cell Transplant
NCT05027945 10000404 000404-C Ph 2 recruiting A Phase II Study of Allogeneic Hematopoietic Stem Cell Transplant for Subjects With VEXAS (Vacuoles, E1 Enzyme, X-linked, Autoinflammatory, Somatic) Syndrome
NCT01861106 130132 13-C-0132 Ph 2 recruiting Allogeneic Hematopoietic Stem Cell Transplant for GATA2 Mutations
NCT07566377 26-168 Ph 2 recruiting Cord Blood Transplantation in Children and Young Adults With Blood Cancer
NCT06962800 PROMINENT 299PN301 2024-519232-16-00 Ph 3 recruiting A Study to Learn More About the Effects and Safety of Felzartamab Infusions in Adults With Primary Membranous Nephropathy (PMN)
NCT03670966 RG1003349 10060, P30CA015704 Ph 1, Ph 2 recruiting 211At-BC8-B10 Followed by Donor Stem Cell Transplant in Treating Patients With Relapsed or Refractory High-Risk Acute Leukemia or Myelodysplastic Syndrome
NCT03816332 results posted NCI-2019-00239 NCI-2019-00239, ETCTN10214 Ph 1 active not recruiting Tacrolimus, Nivolumab, and Ipilimumab in Treating Kidney Transplant Recipients With Selected Unresectable or Metastatic Cancers
NCT06195891 23343 NCI-2023-08816, 23343 Ph 1 recruiting Orca-T Following Chemotherapy and Total Marrow and Lymphoid Irradiation for the Treatment of Acute Myeloid Leukemia, Acute Lymphoblastic Leukemia or Myelodysplastic Syndrome
NCT06807606 2024-1605 NCI-2025-00794 Ph 2 recruiting Optimized Cord Blood Transplantation for the Treatment of Patients With High-risk Hematologic Malignancies Who Have Relapsed After First Allogeneic Stem Cell Transplantation
NCT07412470 FREXERA EFC18554 2025-521521-33-00 Ph 2, Ph 3 recruiting A Study to Investigate the Efficacy and Safety of Frexalimab Versus Tacrolimus in Adults Undergoing Kidney Transplantation
NCT07548983 STUDY00028015 NCI-2025-09157, STUDY00028015 Ph 1 not yet recruiting Ruxolitinib With Azacitidine Maintenance for the Treatment of Patients With Acute Myeloid Leukemia Undergoing Reduced Intensity Allogeneic Stem Cell Transplantation
NCT07302776 IRB-82367 Ph 1 not yet recruiting TACrolimus Targeted Immunosuppression Cessation in ALlogeneic HCT
NCT07493538 2025LS162 Ph 2 recruiting MT2025-35 Allogeneic Hematopoietic Stem Cell Transplantation Using Reduced Intensity Conditioning Treosulfan and Fludarabine, With Post-Transplant Cytoxan (PTCy) for the Treatment of Hematological Diseases
NCT07349771 MC230810 24-009803 Ph 2 not yet recruiting Axatilimab Plus Standard of Care Therapy for the Prevention of Graft Versus Host Disease Following Allogeneic Hematopoietic Stem Cell Transplantation in Patients With Hematologic Cancer, ABRAXAS Trial
NCT06828796 NSH 1420 Ph 2 recruiting Early Use of Tacrolimus in HLA-Mismatched Haploidentical Allogeneic Hematopoietic Transplantation With Post-Transplant Cyclophosphamide
NCT04859946 2020-0971 NCI-2021-02784, 2020-0971 Ph 2 active not recruiting Itacitinib for the Prevention of Graft Versus Host Disease
NCT04177004 19214 NCI-2019-06454, 19214 Ph 1 suspended Human Lysozyme Goat Milk for the Prevention of Graft Versus Host Disease in Patients With Blood Cancer Undergoing a Donor Stem Cell Transplant
NCT03856216 results posted 2018-0860 NCI-2019-00531, 2018-0860 Ph 2 terminated Inotuzumab Ozogamicin and Chemotherapy in Treating Patients With Leukemia or Lymphoma Undergoing Stem Cell Transplantation
NCT01384513 results posted 11D.247 2011-31, JT 1795 Ph 2 completed A Two-Step Approach to Reduced Intensity Bone Marrow Transplant for Patients With Hematological Malignancies
NCT04384692 RG1006507 NCI-2020-01626, 10093 Ph 2 active not recruiting Peritransplant Ruxolitinib for Patients With Primary and Secondary Myelofibrosis
NCT03640026 GLITTER CHD045-17 Ph 4 terminated Glucose Disorders Induced by Tacrolimus on Pre Transplantation Endstage Renal Disease Patients
NCT00792948 results posted NCI-2009-00800 NCI-2009-00800, S0805 Ph 2 active not recruiting Combination Chemotherapy With or Without Donor Stem Cell Transplant in Treating Patients With Acute Lymphoblastic Leukemia
NCT06084780 TRANSCAPE CASE7Z23 Ph 2 not yet recruiting Intestinal & Multivisceral Transplantation for Unresectable Mucinous Carcinoma Peritonei (TRANSCAPE)
NCT05736419 23-009 Ph 2 recruiting A Study of Immune Suppression Treatment for People With Sickle Cell Disease or β-Thalassemia Who Are Going to Receive an Allogeneic Hematopoietic Cell Transplantation (HCT)
NCT06478017 DAIT RTB-013 Ph 2 recruiting Belatacept in Heart Transplantation
NCT04629248 MAJESTY WA41937 2020-003233-38, 2023-506525-11-00 Ph 3 active not recruiting A Study Evaluating the Efficacy and Safety of Obinutuzumab in Participants With Primary Membranous Nephropathy
NCT02891603 results posted MCC-18783 5R01HL133823-02 Ph 1, Ph 2 completed A Phase I/II GVHD Prevention Trial Combining Pacritinib With Sirolimus-Based Immune Suppression
NCT03605927 MCC-19305 Ph 1 completed CD40-L Blockade for Prevention of Acute Graft-Versus-Host Disease
NCT02918292 CHAMP results posted BMT CTN 1502 2U10HL069294-11, 5U24CA076518 Ph 2 completed Optimizing Haploidentical Aplastic Anemia Transplantation (BMT CTN 1502)
NCT02333162 IRB14-0709 NCI-2014-02469, IRB14-0709 Ph 1 suspended Intensity Modulated Total Marrow Irradiation, Fludarabine Phosphate, and Melphalan in Treating Patients With Relapsed Hematologic Cancers Undergoing a Second Donor Stem Cell Transplant
NCT04339101 results posted 19576 NCI-2020-01722, 19576 Ph 2 completed Itacitinib, Tacrolimus, and Sirolimus for the Prevention of GVHD in Patients With Acute Leukemia, Myelodysplastic Syndrome, or Myelofibrosis Undergoing Reduced Intensity Conditioning Donor Stem Cell Transplantation
NCT02251821 results posted 9033 NCI-2014-01882, 9033 Ph 2 completed JAK Inhibitor Before Donor Stem Cell Transplant in Treating Patients With Primary or Secondary Myelofibrosis
NCT01659606 12-950 IRB-P00003466 Ph 2 active not recruiting Radiation- and Alkylator-free Bone Marrow Transplantation Regimen for Patients With Dyskeratosis Congenita
NCT03321656 42753 Ph 2, Ph 3 recruiting Impact of Envarsus XR® on Kidney Biopsy Subclinical Rejection and Blood Immunologic Profile
NCT03663335 CIRRUS I results posted CCFZ533A2201 2017-003607-22 Ph 2 completed Study of Efficacy, Safety, Tolerability, Pharmacokinetic (PK) and Pharmacodynamic (PD) of an Anti-CD40 Monoclonal Antibody, CFZ533, in Kidney Transplant Recipients
NCT07214688 Pro2025-0254 FLU-TBI-800-PTCY Ph 2 recruiting Fludarabine and Intermediate-dose TBI Followed by PTCy in Patients Undergoing Allo Transplant for Heme Malignancies
NCT04904588 ACCESS ACCESS Ph 2 active not recruiting HLA-Mismatched Unrelated Donor Hematopoietic Cell Transplantation With Post-Transplantation Cyclophosphamide
NCT03663933 results posted 180135 18-C-0135 Ph 2 active not recruiting Allogeneic Hematopoietic Cell Transplantation for Disorders of T-cell Proliferation and/or Dysregulation
NCT01804634 J12106 NA_00076243, 5P01CA225618-06 Ph 2 recruiting Reduced Intensity Haploidentical BMT for High Risk Solid Tumors
NCT03970096 RG1005364 9749, NCI-2019-03188 Ph 2 recruiting Graft Versus Host Disease-Reduction Strategies for Donor Blood Stem Cell Transplant Patients With Acute Leukemia or Myelodysplastic Syndrome (MDS)
NCT05622318 PRO00046962 Ph 2 active not recruiting De-escalated Cyclophosphamide (PTCy) and Ruxolitinib for Graft-versus-Host Disease (GVHD) Prophylaxis
NCT06872333 2024LS140 Ph 2 recruiting Allo HSCT for High Risk Hemoglobinopathies
NCT06345495 2023-0899 NCI-2024-02814 Ph 2 recruiting High Dose Ruxolitinib and Allogeneic Stem Cell Transplantation in Myelofibrosis Patients With Splenomegaly
NCT04965597 BMTCTN1904 2U10HL069294-11, RG1121820 Ph 2 completed Treosulfan-Based Conditioning Regimen Before a Blood or Bone Marrow Transplant for the Treatment of Bone Marrow Failure Diseases (BMT CTN 1904)
NCT06638879 2023-0687 Ph 1 completed Tacrolimus Toothpaste for Management of Oral Chronic Graft vs. Host Disease (cGVHD)
NCT05707377 ALMOND BGB-3111-309 2022-501147-32-00, CTR20230546 Ph 2, Ph 3 active not recruiting A Study to Examine the Efficacy and Safety of Zanubrutinib Given to Adults With Primary Membranous Nephropathy

Showing 50 of 371 trials

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Key Completed Trials

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Trial Timeline

Full development history with FDA approval milestones

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Understanding FDA Approval Types
Count Type What it means
- ORIG Original approval - drug first enters market
- SUPPL - Efficacy New indication (new disease/condition approved)
- SUPPL - Labeling Label text changes (warnings, dosing updates)
- SUPPL - Manufacturing Production changes (new facility)
- SUPPL - Chemistry Formulation changes (new dosage strength)

Green lines in the timeline show ORIG and Efficacy approvals - the clinically meaningful milestones.

ASTAGRAF XL FDA Label Details

Indications & Usage

FDA Label (PDF)

ASTAGRAF XL is indicated for the treatment of Organ Rejection.

⚠️ BOXED WARNING

WARNING: MALIGNANCIES AND SERIOUS INFECTIONS IN TRANSPLANT PATIENTS; AND INCREASED MORTALITY IN FEMALE LIVER TRANSPLANT PATIENTS • Increased risk for developing serious infections and malignancies with ASTAGRAF XL ® or other immunosuppressants that may lead to hospitalization or death. [see Warnings...

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Data Sources

Data sourced from official FDA and NIH databases. Click links to verify on original sources.