Clinical trial · Interventional
Rosiglitazone in Treating Patients With Newly Diagnosed ACTH-Secreting Pituitary Tumor (Cushing Disease)
An Open Label, Multicenter Study Evaluating the Safety and Efficacy of Short Term (6 Weeks) Rosiglitazone Treatment in Patient's With Cushing's Disease
NCT00612066CI-TRIAL-00046479terminatedPhase 2Results postedClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): Low accrual and funding term ended
Summary
Brief summary (as posted)
RATIONALE: Rosiglitazone may help pituitary tumor cells become more like normal cells, and to grow and spread more slowly. PURPOSE: This phase II trial is studying how well rosiglitazone works in treating patients with newly diagnosed ACTH-secreting pituitary tumor (Cushing disease).
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 |
|---|---|---|---|
| Cushing's Disease | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| rosiglitazone maleate | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Rosiglitazone
- interventionNames
- Drug: rosiglitazone maleate
Primary outcomes (1)
- measure
- Number of Responders
- timeFrame
- 7 weeks
- description
- Definition of Treatment Response * The primary outcome in Cushing's disease will the % responders, a responder is defined as a patient with 2 consecutive 24h urinary free cortisols within the normal reference range in association with no clinical signs of disease progression. * Secondary outcomes will include the % reduction in 24h UFC (derived by comparison of the mean of 2 baseline 24h UFC values with mean of the two lowest consecutive 24h UFC values while on study treatment in association with no clinical signs of disease progression).
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 65 Years
Show eligibility criteria text
DISEASE CHARACTERISTICS: * Clinically demonstrable ACTH-secreting pituitary tumor * Pituitary tumor demonstrated on MRI with and without contrast AND/OR evidence of a central ACTH source following inferior petrosal sinus sampling * Newly diagnosed disease * Biochemically active disease that is not adequately controlled, as demonstrated by the following standard criteria: * Elevated 24-hour urinary-free cortisol levels on at least 2 separate 24-hour urine collections 1 week apart * Lack of suppression of serum cortisol to \< 1.8 μg/dL (at 8 am) following administration of 1 mg of dexamethasone at 11 pm the night before * Measurable plasma ACTH levels * Patient is hypercortisolemic and does not wish to receive alternate steroid-lowering therapy, such as ketoconazole and/or metyrapone * Patients with evidence of optic nerve or chiasm compression on post-operative MRI must have a normal visual field evaluation by Goldman perimetry * No visual field abnormalities * Hypopituitarism\* allowed, as evidenced by any or all of the following: * Subnormal growth hormone (GH) response to arginine/growth hormone-releasing hormone (GHRH) testing (normal response is an increase of \> 4 ng/mL) * Low age-and sex-matched insulin-like growth factor-1 (IGF-1) levels * Low thyroid-stimulating hormone (TSH) levels * Low free triiodothyronine (T3) and free thyroxine (T4) levels * Low estradiol levels * Low luteinizing hormone (LH) and follicle-stimulating hormone (FSH) levels in postmenopausal female patients * Low testosterone, LH, and FSH levels in male patients NOTE: \*Patients who are diagnosed with hypopituitarism will initiate thyroid hormone replacement therapy prior to pituitary surgery as part of routine care. Other hormone replacement, such as sex steroids or growth hormone, will not be initiated during the study. PATIENT CHARACTERISTICS: * Not pregnant or nursing * Fertile patients must use effective contraception (if oral contraception is used, it must be used for ≥ 2 months prior to, during, and for 1 month after completion of study therapy) * No clinically significant renal, hematologic, or hepatic abnormalities * No prior or concurrent medical condition that may interfere with the conduct of the study or the evaluation of its results, in the opinion of the investigator or the DSMB compliance officer * No history of immunocompromise, including HIV positivity by ELISA and western blot * No alcohol or drug abuse within the past 6 months * No blood donation (≥ 400 mL) within the past 2 months * No other active malignant disease within the past 5 years except for basal cell carcinoma or carcinoma in situ of the cervix * No active or suspected acute or chronic uncontrolled infection * No severe osteoporosis, defined as bone mineral density T scores \< 2.5 standard deviations below age-matched controls * No history of noncompliance to medical regimens * Considered reliable * Able to complete the entire study PRIOR CONCURRENT THERAPY: * More than 3 months since prior rosiglitazone or other thiazolidinedione * No prior or concurrent radiotherapy for pituitary tumor * More than 1 month since prior participation in any clinical investigation involving an investigational drug * More than 30 days since prior unlicensed drugs * No concurrent pituitary surgery
References
Publications (0)
Data not yet available
No reference posted for this study.