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About RON

RON, also known as Recepteur d'Origine Nantais, is a receptor tyrosine kinase (RTK) involved in cell growth and survival. RTKs are cell surface receptors; their aberrant activation is frequently observed in cancers, making them therapeutic targets.

1
Approved Drugs
1
Companies
3
Indications
1
Therapeutic Areas
Broadest Approval
XALKORI
PF PRISM CV
3
approved indications

Top RON Drugs

XALKORI
PF PRISM CV
3 indications · 2011
🏢

The competitive landscape is limited, with only one company, PF PRISM CV, having an approved drug.

RON Drug Modality Landscape

Modalities

Small molecule
1
100%

Routes of Administration

💊 Oral
1
100%
💡

Only one approved drug targets RON, using small molecule modality.

Explore opportunities for novel modalities like antibodies or PROTACs to target RON.

Oral option available Small molecules only

RON Clinical Trials 85 trials

Phase 1-4 trials started in 2008 or later that test an FDA-approved drug acting on RON. Source: ClinicalTrials.gov. How we count

85
Total Trials
27
Active
44
Completed
76%
Completion Rate

Completion by Phase

Phase Total Completed Stopped Active Completion
Phase 1 33 25 6 2 81%
Phase 2 34 14 6 14 70%
Phase 3 15 5 0 10 100%
Phase 4 3 0 2 1 0%

Top Sponsors

Pfizer 24 73%
National Cancer Institute (N... 9 50%
Hoffmann-La Roche 4 100%
M.D. Anderson Cancer Center 4 67%
IDEAYA Biosciences 3
Hunan Province Tumor Hospital 3
Bristol-Myers Squibb 2 100%
Children's Oncology Group 2 100%

By Modality

Small molecule
85 76%
Source: ClinicalTrials.gov · Completion rate = completed ÷ (completed + terminated + withdrawn)

Phase 3 Readout Calendar Pro

3 Phase 3 trials testing approved RON drugs across all sponsors.

Full calendar →
Q1 2027
IDE196
IDEAYA Biosciences · Metastatic Uveal Melanoma
Estimated · aging NCT05987332
Q2 2028
Entrectinib
Hoffmann-La Roche · Carcinoma, Non-Small-Cell Lung
Estimated · aging NCT04603807
Q1 2029
Taletrectinib
Nuvation Bio Inc. · Non Small Cell Lung Cancer
Estimated · aging NCT06564324

Coverage: trials whose intervention is an approved drug targeting RON. Pre-approval candidates with development codes (e.g. AZD0901, MK-7240) are not yet linked. Anchored on CT.gov primary completion date.

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Competitive Landscape

  • • 1 companies competing
  • • Market share by company

Full Drug Portfolio

  • • All 1 approved drugs
  • • Approval dates & indications

Genetic Validation

  • • Full genetic evidence table
  • • Effect sizes & directions

Approval Timeline

  • • Full 1-drug timeline
  • • First-of-modality markers

Clinical Trials Analysis

  • • Sponsors: 42 (10 companies)
  • • Completion rates by condition
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Full summary • All drugs • Genetic evidence • Trials • Timeline

How We Count Trials

  • Trials: phase 1-4 interventional trials on ClinicalTrials.gov that started in 2008 or later and test an FDA-approved drug acting on RON. A trial counts if an approved drug acting on RON is in any arm, including as a comparator, and a trial that tests two such drugs counts once. Trials that test only unapproved drugs are not counted. A trial listed as phase 1/2 counts as phase 1, and phase 2/3 as phase 2.
  • Active: recruiting, not yet recruiting, enrolling by invitation, or active and no longer recruiting.
  • Completion rate: of the trials that have ended, the share marked Completed rather than Terminated or Withdrawn. Completed means the trial ended as planned; it does not mean the drug worked. Suspended trials are not counted as ended.
  • Stopped: terminated or withdrawn. Trials stop for many reasons, including slow enrolment and business decisions, not only safety or efficacy.
  • Sponsors: the lead sponsor of each trial. Companies are the sponsors ClinicalTrials.gov classes as industry; the rest are universities, hospitals, cooperative groups, government bodies and individuals.