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NCT06668493: LUNAR

Low-grade UTUC Treated With Nadofaragene Firadenovec Administered to Renal Pelvis

Recruiting now Phase 1, PHASE2 Last updated 27 February 2026
What this trial tests

Phase 1, PHASE2 trial testing Nadofaragene Firadenovec in Low-grade Upper Tract Urothelial Carcinoma in 20 participants. Currently enrolling.

Timeline
12 June 2025
Primary endpoint
30 November 2029
30 November 2029

Quick facts

Lead sponsorFerring Pharmaceuticals
PhasePhase 1, PHASE2
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment20
Start date12 June 2025
Primary completion30 November 2029
Estimated completion30 November 2029
Sites7 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Ferring Pharmaceuticals — full company profile →

Who can join

18 and older, any sex, with Low-grade Upper Tract Urothelial Carcinoma. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The primary purpose of this trial is to evaluate the safety \& tolerability of Nadofaragene Firadenovec in subjects with LG-UTUC. To help with this evaluation, a safety lead-in period will be conducted for the first 6 subjects. Complete response is at 3 or 6 months defined as absence of any UTUC in the renal pelvis.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Clinical Trials and Emerging Therapeutic Paradigms in Upper-Tract Urothelial Carcinoma.
    Chavarriaga J, Raman JD. · · 2026 · PMID 42073550 · DOI 10.3390/cancers18081223

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Other trials of Nadofaragene Firadenovec

Trials testing the same drug.

Other Ferring Pharmaceuticals trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06668493.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing