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Renal Cell Carcinoma

Oncology 5 original drugs
5
Novel Drugs
7
Reformulations
301
Active Trials
33
Drug Targets

Phase 3 Readouts Pro

7 active Phase 3 trials with confidence-graded completion dates.

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Q2 2026
89Zr-TLX250 PET/CT
Telix Pharmaceuticals (Innovations) Pty Limited
Estimated · stale NCT06750419
Q4 2026
Pazopanib
Xynomic Pharmaceuticals, Inc.
Estimated · stale NCT03592472
Q1 2027
Nivolumab
Bristol-Myers Squibb
Estimated · fresh NCT03873402
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Anchored on CT.gov primary completion date. Topline announcements typically precede this by 3–9 months. Confidence labels combine date type (ACTUAL/ESTIMATED) with last-update freshness.

Treatments by Mechanism

Top 9 mechanisms across 44 industry trials with a known mechanism of action.

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Hypoxia-inducible Factor Inhibitor
7 trials 7 active 2 sponsors
Programmed Death Receptor-1 Blocking Antibody
22 trials 2 active 4 sponsors
AXL/FLT-3/KIT/MER/MET/RET/ROS1/TIE-2/TRKB/TYRO3/VEGFR-1/VEGFR-2/VEGFR-3
4 trials 2 active 3 sponsors
ALK/ROS1/NTRK1/TRKB/TRKC
1 trials 1 active 1 sponsor
Kinase Inhibitor
6 trials 6 sponsors
Lymphocyte Growth Factor
1 trials 1 sponsor
Vascular Endothelial Growth Factor Inhibitor
1 trials 1 sponsor
RANK Ligand Inhibitor
1 trials 1 sponsor
Thalidomide Analog
1 trials 1 sponsor

MoA derived from FDA pharmClassEpc when intervention matches an approved drug. Codenamed clinical-stage assets without an approved counterpart show "—" and aren't grouped here — they're still in the phase tables below.

Clinical Pipeline by Phase

307 industry-sponsored trials across 154 sponsors

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Precision Medicine Biomarkers

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Biomarkers used for patient selection in Renal Cell Carcinoma

Reformulations (7 drugs) Click to expand

Reformulations are FDA-approved versions of existing molecules in new dosage forms (e.g., oral solution vs tablet, extended-release vs immediate-release). They require a new NDA but use an already-proven active ingredient.

Generic Drugs (4 ANDA approved) Click to expand

Generic drugs contain the same active ingredient as the brand-name drug and are approved via ANDA (Abbreviated New Drug Application).

Related Indications

Other Oncology indications

Drug Categories:

  • Novel Drugs: NDA Type 1/2 (new molecular entity) or original BLA
  • Reformulations: NDA Type 3/5 (new dosage form of existing molecule)
  • Biosimilars: BLA-approved biologics highly similar to reference products
  • Generics: ANDA-approved copies of small molecule drugs

View data sources and methodology