TheraRadar

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Data updated: Mar 10, 2026

PHYRAGO

DASATINIB
Oncology Approved 2023-12-05
2
Indications
--
Phase 3 Trials
2
Years on Market

Details

Status
Prescription
First Approved
2023-12-05
Routes
ORAL
Dosage Forms
TABLET

Companies

Active Ingredient: DASATINIB

PHYRAGO Approval History

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What PHYRAGO Treats

2 indications

PHYRAGO is approved for 2 conditions since its original approval in 2023. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Chronic Myeloid Leukemia
  • Acute Lymphoblastic Leukemia
Source: FDA Label

PHYRAGO Target & Pathway

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Target

BCR-ABL (Breakpoint Cluster Region-Abelson) Fusion Protein

An abnormal fusion protein created by a chromosomal translocation, found in chronic myeloid leukemia (CML). BCR-ABL has constitutive kinase activity that drives leukemic cell proliferation. Targeting BCR-ABL transformed CML from a fatal disease to a manageable condition.

PHYRAGO Competitors

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4 other drugs also target BCR-ABL. Compare mechanisms, indications, and trial activity.

Drug = Competitor name Company = Manufacturer N indic. = FDA-approved indications → Date = Patent/exclusivity expiry

Competitors share the same molecular target (BCR-ABL). Earlier expiry dates signal biosimilar/generic opportunities.

Drugs Similar to PHYRAGO

FDA-approved drugs for similar conditions. Compare mechanisms and indications to understand treatment alternatives.

DASATINIB
DASATINIB
2 shared
Apotex
Shared indications:
Chronic Myeloid LeukemiaAcute Lymphoblastic Leukemia
IMKELDI
IMATINIB MESYLATE
2 shared
SHORLA ONCOLOGY
Shared indications:
Chronic Myeloid LeukemiaAcute Lymphoblastic Leukemia
SPRYCEL
DASATINIB
2 shared
Bristol-Myers Squibb
Shared indications:
Chronic Myeloid LeukemiaAcute Lymphoblastic Leukemia
ASPARLAS
CALASPARGASE PEGOL-MKNL
1 shared
SERVIER PHARMA LLC
Shared indications:
Acute Lymphoblastic Leukemia
BESPONSA
INOTUZUMAB OZOGAMICIN
1 shared
Pfizer
Shared indications:
Acute Lymphoblastic Leukemia
BLINCYTO
BLINATUMOMAB
1 shared
Amgen
Shared indications:
Acute Lymphoblastic Leukemia
CLOFARABINE
CLOFARABINE
1 shared
PHARMOBEDIENT
Shared indications:
Acute Lymphoblastic Leukemia
DANZITEN
NILOTINIB TARTRATE
1 shared
AZURITY
Shared indications:
Chronic Myeloid Leukemia
DOXIL (LIPOSOMAL)
DOXORUBICIN HYDROCHLORIDE
1 shared
Baxter
Shared indications:
Acute Lymphoblastic Leukemia
DOXORUBICIN HYDROCHLORIDE (LIPOSOMAL)
DOXORUBICIN HYDROCHLORIDE
1 shared
AYANA PHARMA LTD
Shared indications:
Acute Lymphoblastic Leukemia
ELSPAR
ASPARAGINASE
1 shared
Merck
Shared indications:
Acute Lymphoblastic Leukemia
HYDREA
HYDROXYUREA
1 shared
WAYLIS THERAP
Shared indications:
Chronic Myeloid Leukemia
HYDROXYUREA
HYDROXYUREA
1 shared
LEADING
Shared indications:
Chronic Myeloid Leukemia
ICLUSIG
PONATINIB HYDROCHLORIDE
1 shared
Takeda
Shared indications:
Chronic Myeloid Leukemia
JYLAMVO
METHOTREXATE
1 shared
SHORLA
Shared indications:
Acute Lymphoblastic Leukemia
MERCAPTOPURINE
MERCAPTOPURINE
1 shared
Viatris
Shared indications:
Acute Lymphoblastic Leukemia
METHOTREXATE SODIUM PRESERVATIVE FREE
METHOTREXATE SODIUM
1 shared
Hikma
Shared indications:
Acute Lymphoblastic Leukemia
ONCASPAR
PEGASPARGASE
1 shared
SIGMA TAU
Shared indications:
Acute Lymphoblastic Leukemia
PURINETHOL
MERCAPTOPURINE
1 shared
STASON PHARMS
Shared indications:
Acute Lymphoblastic Leukemia
PURIXAN
MERCAPTOPURINE
1 shared
NOVA LABS LTD
Shared indications:
Acute Lymphoblastic Leukemia
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Active Pipeline

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Ongoing clinical trials by development phase

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Key Completed Trials

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Completed studies with published results, ranked by significance

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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.

PHYRAGO FDA Label Details

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Indications & Usage

FDA Label (PDF)

PHYRAGO is indicated for the treatment of adult patients with newly diagnosed Philadelphia chromosome-positive (Ph+) chronic myeloid leukemia (CML) in chronic phase. chronic, accelerated, or myeloid or lymphoid blast phase Ph+ CML with resistance or intolerance to prior therapy including imatinib. Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ ALL) with resistance or intolerance to prior therapy. PHYRAGO is indicated for the treatment of pediatric patients 1 year of age and older with Ph+ CML in chronic phase. newly diagnosed Ph+ ALL in combination with chemotherapy. PHYRAG...

PHYRAGO Patents & Exclusivity

Latest Patent: Jan 2041
Exclusivity: Dec 2026

Patents (504 active)

US11324745 Expires Jan 22, 2041
US11202778 Expires Jan 22, 2041
US12433891 Expires Jan 22, 2041
US12465606 Expires Jan 22, 2041
US11298356 Expires Jan 22, 2041
+ 494 more patents

Exclusivity

M-307 Until Dec 2026
M-307 Until Dec 2026
M-307 Until Dec 2026
M-307 Until Dec 2026
M-307 Until Dec 2026
Source: FDA Orange Book

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Data Sources

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