Clinical trial · Interventional
Suramin in Treating Patients With Recurrent Bladder Cancer
A Phase I Study of Intravesicular Suramin in Recurrent Superficial Bladder Cancer
NCT00006476CI-TRIAL-00011052completedPhase 1ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
RATIONALE: Suramin may stop the growth of bladder cancer by stopping blood flow to the tumor. PURPOSE: Phase I trial to study the effectiveness of suramin in treating patients who have recurrent bladder cancer.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Bladder Cancer | Malignant Bladder Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| conventional surgery | Procedure | — | UNRESOLVED |
| suramin | Drug | — | UNRESOLVED |
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
DISEASE CHARACTERISTICS:
* Histologically proven recurrent superficial bladder cancer
* Intermediate prognosis as defined by the following:
* Recurrent, multiple Ta, T1 carcinoma
* Multiple (1-7) tumors
* Tumors resected previously must be histological grade G1 or G2 OR
* Previously treated superficial bladder cancer requiring followup cystoscopy
* Recurrent disease diagnosed at surgery
* No tumor invasion into muscle or carcinoma in situ
PATIENT CHARACTERISTICS:
Age:
* 18 and over
Performance status:
* WHO 0-2
Life expectancy:
* Not specified
Hematopoietic:
* WBC at least 3,500/mm3
* Platelet count at least 150,000/mm3
Hepatic:
* No clinically significant hepatic disease
Renal:
* Creatinine clearance greater than 60 mL/min
Other:
* Not pregnant or nursing
* Negative pregnancy test
* Fertile patients must use effective contraception during and for 6 months after study
* No history of adrenal insufficiency
* No other malignancy within the past 5 years except adequately treated cone-biopsied carcinoma in situ of the cervix or nonmelanoma skin cancer
* No history of difficult catheterization
* No confusion or disorientation
* No other condition that would preclude study compliance
PRIOR CONCURRENT THERAPY:
Biologic therapy:
* No concurrent biologic therapy
Chemotherapy:
* No concurrent chemotherapy
Endocrine therapy:
* No concurrent corticosteroids
Radiotherapy:
* No prior radiotherapy to the bladder
* No concurrent radiotherapy
Surgery:
* See Disease Characteristics
* At least 4 weeks since prior major thoracic or abdominal surgery
Other:
* Recovered from prior therapy and stable for 4 weeks
* At least 6 weeks since prior intravesicular therapy
* No prior or concurrent investigational drugs
* No concurrent anticoagulantsReferences
Publications (1)
- RESULTOrd JJ, Streeter E, Jones A, Le Monnier K, Cranston D, Crew J, Joel SP, Rogers MA, Banks RE, Roberts IS, Harris AL. Phase I trial of intravesical Suramin in recurrent superficial transitional cell bladder carcinoma. Br J Cancer. 2005 Jun 20;92(12):2140-7. doi: 10.1038/sj.bjc.6602650. PMID 15928663