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NCT00629642: SONIC
Clinical Study of Solifenacin Succinate in Patients With Bladder Symptoms Due to Spinal Cord Injury or Multiple Sclerosis
Phase 4 trial testing Solifenacin Succinate in Multiple Sclerosis in 249 participants. Completed in 28 January 2011.
28 January 2011
Quick facts
| Lead sponsor | Astellas Pharma Inc |
|---|---|
| Phase | Phase 4 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | quadruple |
| Primary purpose | treatment |
| Enrollment | 249 |
| Start date | 14 March 2008 |
| Primary completion | 28 January 2011 |
| Estimated completion | 28 January 2011 |
| Sites | 39 locations across France, Italy, Netherlands, Russia, Belgium, United Kingdom, Germany, Hungary |
Drugs / interventions tested
- Solifenacin Succinate — full drug profile →
- Solifenacin Succinate — full drug profile →
- Oxybutynin Hydrochloride
- Placebo
Conditions studied
- Multiple Sclerosis — all drugs for Multiple Sclerosis →
- Neurogenic Bladder — all drugs for Neurogenic Bladder →
- Spinal Cord Diseases — all drugs for Spinal Cord Diseases →
Sponsor
Astellas Pharma Inc — full company profile →
Who can join
Adults 18 to 65, any sex, with Multiple Sclerosis or Neurogenic Bladder. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
A clinical study to evaluate the efficacy and safety of solifenacin in patients with bladder symptoms due to spinal cord injury or multiple sclerosis
Publications & conference data
2 peer-reviewed publications reference this trial (live from Europe PMC):
-
A high throughput drug screening assay to identify compounds that promote oligodendrocyte differentiation using acutely dissociated and purified oligodendrocyte precursor cells.
Lariosa-Willingham KD, Rosler ES, Tung JS, Dugas JC, et al · · 2016 · cited 52× · PMID 27592856 · DOI 10.1186/s13104-016-2220-2 -
Development of a high throughput drug screening assay to identify compounds that protect oligodendrocyte viability and differentiation under inflammatory conditions.
Lariosa-Willingham KD, Rosler ES, Tung JS, Dugas JC, et al · · 2016 · cited 6× · PMID 27629829 · DOI 10.1186/s13104-016-2219-8
Verify or expand the search:
- PubMed search for NCT00629642
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other trials of Solifenacin Succinate
Trials testing the same drug.
- NCT06201013 — Vitamin D Treat-to-Target Strategy for Children With Overactive Bladder-Wet · NA · recruiting
- NCT01747577 — Post Marketing Study to Evaluate the Efficacy and Safety of Solifenacin in Patients With OAB (Overactive Bladder) After · Phase 4 · completed
Other recruiting trials for Multiple Sclerosis
Currently open trials in the same condition.
- NCT07507084 — The Effect of Internal- or External-Focused Exercise Training, Administered in Conjunction With a Cognitive Task, on Wal · NA · recruiting
- NCT07524231 — Evaluation of the Effects of Laughter Yoga · NA · recruiting
- NCT07489794 — URINARY INCONTINENCE AND PELVIC FLOOR MUSCLE ACTIVITY IN MULTIPLE SCLEROSIS · recruiting
- NCT07236684 — Identification of Factors Related to UI in Patients With MS and EMG Assessment of PFM Activity · recruiting
- NCT07500727 — Skeletal Muscle Aging and Responsiveness in Aged People With MS · NA · recruiting
Other Astellas Pharma Inc trials
Trials by the same sponsor.
- NCT07318714 — A Study of ASP2246 for People Who Have Movement Problems Caused by Brain Injury After a Stroke · Phase 1, PHASE2 · recruiting
- NCT07094204 — A Study to Find a Suitable Dose of ASP5834 in Adults With Solid Tumors · Phase 1 · recruiting
- NCT06970665 — A Study About the Safety of ASP3021 Eye Injections and if They Help People in Japan With Vision Loss From Age-related Ma · Phase 4 · recruiting
- NCT06364696 — A Study to Find a Suitable Dose of ASP4396 in Adults With Solid Tumors · Phase 1 · active not recruiting
- NCT06206421 — A Study to Assess Long-term Safety of Fezolinetant Given to Japanese Women Going Through Menopause · Phase 3 · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT00629642 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 9 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Astellas Pharma Inc
- Last refreshed: 14 November 2024
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/NCT00629642.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing