Topsalysin
drugOn this page
Also known as PRX-302PRX302TopsalisinaTopsalysine
Summary
Topsalysin (CHEMBL2364656) is a phase-3 clinical-stage unknown; indicated across 2 conditions including benign prostatic hyperplasia.
At a glance
- Status: Max clinical phase 3 (not approved)
- Modality: Unknown
- Indications: 2 conditions
- Clinical trials: 6
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL2364656 |
| Name | Topsalysin |
| Type | Unknown |
| Max phase | 3 |
Also known as: PRX-302, PRX302, Topsalisina, Topsalysin, Topsalysine, TOPSALYSIN
Targets
Targets
No target linkage available.
Bioactivity
No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).
Target pathways
No target-pathway data for this drug (no mapped target genes).
Indications & clinical
Indications
2 indications (0 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).
| Indication | Trial phase | MONDO | EFO |
|---|---|---|---|
| benign prostatic hyperplasia | 3 | MONDO:0010811 | EFO:0000284 |
1 further indication record had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.
Clinical trials
Total trials: 6.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE2 | 4 |
| PHASE3 | 1 |
| PHASE1/PHASE2 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT01966614 | PHASE3 | COMPLETED | Randomized, Double-Blind, Vehicle-Controlled, Multicenter Safety and Efficacy Study of Intraprostatic PRX302 for LUTS BPH |
| NCT00686088 | PHASE2 | COMPLETED | An Open-Label, Multi-Center, Phase IIa Trial of PRX302 Treatment of Patients With Locally Recurrent Prostate Cancer After Primary Radiation Therapy |
| NCT00889707 | PHASE2 | COMPLETED | Transperineal Intraprostatic Injection of PRX302 Under Ultrasound Guidance for Management of Prostatic Hyperplasia |
| NCT01454349 | PHASE1/PHASE2 | COMPLETED | Study of PRX302 for Lower Urinary Tract Symptoms Due to Benign Prostatic Hyperplasia (BPH) |
| NCT02499848 | PHASE2 | COMPLETED | Evaluate, Safety and Tolerability of Intraprostatic PRX302 Administration, Low to Intermediate Risk Prostate Cancer |
| NCT03081481 | PHASE2 | COMPLETED | Intraprostatic PRX302 Injection to Treat Localised Prostate Cancer |
Clinical evidence (CIViC)
No CIViC predictive evidence (expected for non-precision-medicine drugs).
Pharmacology
Pharmacogenomics
No PharmGKB pharmacogenomic data curated for this drug.
Related molecules
Related molecules
No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).
Related Atlas pages
- Diseases: benign prostatic hyperplasia