Clinical trial · Interventional
Sulindac Capsules Compared With Sulindac Tablets in Healthy Volunteers
Bioequivalency Study of Sulindac in Capsule vs. Tablet Formulations
NCT00343629CI-TRIAL-00017672completedN/AClinicalTrials.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: Giving healthy volunteers sulindac capsules or sulindac tablets may help doctors learn which form of the drug may be more effective in preventing cancer. PURPOSE: This randomized clinical trial is studying sulindac capsules to see how well they work compared with sulindac tablets in healthy volunteers.
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 |
|---|---|---|---|
| Unspecified Adult Solid Tumor, Protocol Specific | Adult Solid Neoplasm | ALIAS | 0.85 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| pharmacological study | Other | — | UNRESOLVED |
| sulindac | Drug | Sulindac | ALIAS |
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 40 Years
Show eligibility criteria text
DISEASE CHARACTERISTICS:
* Healthy volunteer
PATIENT CHARACTERISTICS:
* ECOG performance status 0-2
* Not pregnant or nursing
* Negative pregnancy test
* Fertile patients must use effective contraception
* Hemoglobin ≥ 12.0 g/dL (women)
* Hemoglobin ≥ 13.5 g/dL (men)
* WBC \> 3,000/mm³
* Platelet count \> 100,000/mm³
* Absolute neutrophil count \> 1,500/mm³
* Alkaline phosphatase ≤ 1.5 times upper limit of normal (ULN)
* Bilirubin ≤ 1.5 times ULN
* ALT ≤ 1.5 times ULN
* Creatinine ≤ 1.5 times ULN OR creatinine clearance ≥ 30 mL/min
* No history of allergic reactions or hypersensitivity to sulindac or other NSAIDs, including aspirin-sensitive asthma or urticaria
* No condition that interferes with ingestion or absorption of oral medications
* No cancer within the past 3 years except nonmelanomatous skin cancer, localized prostate cancer, carcinoma in situ of the cervix, or superficial bladder cancer that was previously treated \> 6 months ago
* No uncontrolled concurrent illness including, but not limited to, the following:
* Ongoing or active infection
* Symptomatic congestive heart failure
* Unstable angina pectoris
* Cardiac arrhythmia
* Myocardial infarction in the past 6 months
* Chronic renal disease
* Chronic liver disease
* Hypertension that is difficult to control
* Psychiatric illness or social situations that would limit study compliance
* No other significant clinical disorder or laboratory finding that would preclude study participation
* No consumption of alcoholic or caffeinated beverages for ≥ 24 hours prior to study drug administration and until all blood samples have been drawn
* Willing to provide required biologic specimens
PRIOR CONCURRENT THERAPY:
* More than 6 months since prior investigational agents
* More than 6 months since prior regular use of (defined as a frequency of 7 consecutive days for \> 3 weeks or \> 21 days total) or other concurrent nonsteroidal anti-inflammatory drugs (NSAIDs) or cyclooxygenase (COX)-2 inhibitors including, but not limited to, the following:
* Ibuprofen
* Ketoprofen
* Naproxen
* More than 6 weeks since prior oral corticosteroids
* More than 30 days since prior and no concurrent use of any of the following:
* Methotrexate
* Corticosteroids
* Warfarin
* Ticlopidine
* Clopidogrel
* Low molecular weight heparins
* Abciximab
* Dipyridamole
* Eptifibatide
* Tirofiban
* Lithium
* Cyclosporine
* Hydralazine
* Angiotensin-converting enzymes (ACE) inhibitors
* ACE-receptor antagonists allowed
* Angiotensin-receptor blockers
* Ginkgo
* Ketorolac
* Levofloxacin
* Loop diuretics
* Meadowsweet
* Selective serotonin reuptake inhibitors
* Danaparoid
* No concurrent regular aspirin use unless prescribed by a physician for prevention
* A maximum of one aspirin (81 mg/day) allowed
* No concurrent herbal products (e.g., saw palmetto or Hypericum perforatum \[St. John's wort\])References
Publications (0)
Data not yet available
No reference posted for this study.