Last reviewed · How we verify

NCT07410455

An Open-label, Phase 2 Pilot Study on the Efficacy and Safety of Piclidenoson in Patients With Lowe Syndrome

Not yet recruiting Phase 2 Last updated 18 February 2026
What this trial tests

Phase 2 trial testing Piclidenoson in Lowe Syndrome in 5 participants. Not yet recruiting.

Timeline
1 June 2026
Primary endpoint
31 August 2027
31 August 2027

Quick facts

Lead sponsorCan-Fite BioPharma
PhasePhase 2
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment5
Start date1 June 2026
Primary completion31 August 2027
Estimated completion31 August 2027
Sites1 location across Italy

Drugs / interventions tested

Conditions studied

Sponsor

Can-Fite BioPharma — full company profile →

Who can join

18 and older, male only, with Lowe Syndrome. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The primary objective of this trial is to: 1\. Evaluate the efficacy of piclidenoson to increase renal uptake of 99mTc-labeled DMSA, in comparison to baseline, after 6 months (26 weeks) of treatment as a measure the reabsorption capacity of LMWPs by renal proximal tubules. The secondary objectives of this trial are to: 1. Evaluate changes in urinary excretion of LMWPs and other clinical parameters of renal Fanconi syndrome 2. Evaluate safety of piclidenoson in patients with Lowe syndrome

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

Other trials of Piclidenoson

Trials testing the same drug.

Other recruiting trials for Lowe Syndrome

Currently open trials in the same condition.

Other Can-Fite BioPharma 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/NCT07410455.

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