TheraRadar
Data updated: May 26, 2026

GAVRETO (pralsetinib)

Rearranged during Transfection (RET) Inhibitors Genetically Validated Trial Activity: Growth 5 active trials
Orphan Drug Breakthrough Therapy Priority Review Accelerated Approval
Oncology Approved 2020-09-04

GAVRETO is indicated for the treatment of Metastatic RET fusion-positive non-small cell lung cancer; Advanced or metastatic RET fusion-positive thyroid cancer.

Source: FDA Label • RIGEL PHARMS • Kinase Inhibitor

How GAVRETO Works

Pralsetinib is a kinase inhibitor that targets wild-type RET as well as various oncogenic RET fusions and mutations. These genetic alterations can hyperactivate downstream signaling pathways, which leads to the uncontrolled proliferation of cancer cells. By inhibiting these specific proteins, the drug demonstrates anti-tumor activity and reduces the tumorigenic potential in cancers harboring RET fusions or mutations.

Development Insights

Hoffmann-La Roche conducting 3 trials (38%)
25 indications explored (Broad Platform)
non-small cell lung cancer (1 trials)
solid tumors (1 trials)
ret-fusion non small cell lung cancer (1 trials)
3
Indications
--
Phase 3 Trials
2
Priority Reviews
5
Years on Market

Details

Status
Prescription
First Approved
2020-09-04
Patent Cliff
2042

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Patent cliff and revenue data

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Routes
ORAL
Dosage Forms
CAPSULE

Companies

Active Ingredient: PRALSETINIB

GAVRETO Approval History

2021
2022
2023
2024
2025
2026
Original
New Indication
New Form
Label Update
11 FDA actions from 2020 to 2025 · 1 indication expansions
Dec 2025 SUPPL
Label · Labeling
Mar 2024 SUPPL
Label · Labeling
Aug 2023 SUPPL
Efficacy

What GAVRETO Treats

2 indications

GAVRETO is approved for 2 conditions since its original approval in 2020. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Metastatic RET fusion-positive non-small cell lung cancer
  • Advanced or metastatic RET fusion-positive thyroid cancer
Source: FDA Label

GAVRETO Boxed Warning

SERIOUS INFECTIONS, INCLUDING OPPORTUNISTIC INFECTIONS GAVRETO may increase the risk for serious infections, including bacterial, fungal, viral and opportunistic infections, which can lead to hospitalization or death. Withhold, reduce the dose or permanently discontinue GAVRETO based on severity [see Dosage and Administration (2.3) , Warnings and Precautions (5.1) ] . WARNING: SERIOUS INFECTIONS, INCLUDING OPPORTUNISTIC INFECTIONS See full prescribing information for complete boxed warning. GAVR...

GAVRETO Target & Pathway

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Target

FGFR1 ()

GAVRETO Competitive Set

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Three rings of competition based on shared molecular targets and treated indications.

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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

8 trials
Trial Sponsor ID Phase Status Title
NCT04589845 BO41932 2020-001847-16, 2023-507418-28-00 Ph 2 active not recruiting Tumor-agnostic Precision Immuno-oncology and Somatic Targeting Rational for You (TAPISTRY) Platform Study
NCT06563999 NUMER GASTO-10117 Ph 2 recruiting Neoadjuvant Umbrella Trial for Patients With Unresectable Stage III NSCLC Harboring Rare Mutations.
NCT04302025 ML41591 Ph 2 recruiting A Study of Multiple Therapies in Biomarker-selected Participants With Resectable Stages IB-III Non-small Cell Lung Cancer (NSCLC)
NCT04222972 AcceleRET-Lung results posted BO42864 2019-002463-10, BLU-667-2303 Ph 3 terminated A Study of Pralsetinib Versus Standard of Care for First-Line Treatment of Advanced Non-Small Cell Lung Cancer (NSCLC)
NCT07010393 Real-Neo Ph 4 not yet recruiting Genotype-Driven Neoadjuvant Therapy for Locally Advanced Thyroid Cancer: A Real-World Cohort Study
NCT04632992 MyTACTIC results posted ML42439 Ph 2 completed A Study Evaluating Targeted Therapies in Participants Who Have Advanced Solid Tumors With Genomic Alterations or Protein Expression Patterns Predictive of Response
NCT06482086 202314711 Ph 2 recruiting Efficacy of Organoid-Based Drug Screening to Guide Treatment for Locally Advanced Thyroid Cancer
NCT04760288 AcceleRET-MTC CO42865 2020-005269-15 Ph 3 withdrawn A Study of Pralsetinib Versus Standard of Care (SOC) for Treatment of RET-Mutated Medullary Thyroid Cancer (MTC).
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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.

GAVRETO FDA Label Details

Indications & Usage

FDA Label (PDF)

GAVRETO is indicated for the treatment of Metastatic RET fusion-positive non-small cell lung cancer; Advanced or metastatic RET fusion-positive thyroid cancer.

⚠️ BOXED WARNING

WARNING: SERIOUS INFECTIONS, INCLUDING OPPORTUNISTIC INFECTIONS GAVRETO may increase the risk for serious infections, including bacterial, fungal, viral and opportunistic infections, which can lead to hospitalization or death. Withhold, reduce the dose or permanently discontinue GAVRETO based on sev...

View full patent landscape →
4 OB patents · 2 families · 108 international docs across 35 countries

GAVRETO Patents & Exclusivity

Latest Patent: Jul 2042
Exclusivity: Dec 2027

Patents (6 active)

US12448366 Expires Jul 7, 2042
US11273160 Expires Apr 3, 2039
US12539303 Expires Apr 3, 2039
US11872192 Expires Apr 3, 2039
US11963958 Expires Apr 3, 2039
US10030005 Expires Nov 1, 2036

Exclusivity

ODE-318 Until Sep 2027
ODE-340 Until Dec 2027
ODE-341 Until Dec 2027
Source: FDA Orange Book

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Revenue Insights

  • Quarterly revenue tracking
  • Historical trend analysis

Patent Timeline

  • Cliff: 2042
  • 7 active patents

Trial Analysis

  • 8 total trials
  • Stage: Growth

Competitive Landscape

  • Competitor tracking
  • Same target/indication analysis
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Full approval history • All patents • Revenue trends • Competitor analysis

Data Sources

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

How We Calculate These Metrics

Trial Activity Stage

Measures the current development activity pattern based on trial phases, status, and trends. Important: This measures R&D activity, not commercial lifecycle.

Trial statuses: "Active" means recruiting or ongoing. "Completed" means reached planned endpoint. "Terminated" means stopped early—often due to safety, efficacy, or business reasons.

  • Growth: High proportion of early-phase trials (Phase 1/2), active development
  • Expansion: Significant Phase 3 activity, approaching or pursuing approvals
  • Mature: Substantial Phase 4 post-marketing studies
  • Stable: Mixed phase distribution, steady development
  • Declining: Low active trial ratio, reduced R&D investment