Clinical trial · Interventional
Endostatin in Treating Patients With Advanced Solid Tumors
A Phase I Surrogate Endpoint Trial of Human Recombinant Endostatin in Patients With Advanced Solid Tumors Amenable to Biopsy
NCT00004229CI-TRIAL-00009410completedPhase 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)
Phase I trial to study the effectiveness of endostatin in treating patients who have advanced solid tumors. Endostatin may stop the growth of cancer by stopping blood flow to the tumor.
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 (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| recombinant human endostatin | Biological | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Arm I
- description
- Patients undergo a biopsy during prestudy and after the second course of treatment. Patients receive endostatin IV daily for 4 weeks. Patients on dose level 1-6 receive endostatin over 20 minutes. Patients on dose level 7 receive endostatin over 40 minutes, with no treatment on day 2 of the first course only. Treatment continues every 4 weeks in the absence of disease progression or unacceptable toxicity. Cohorts of 3-6 patients receive escalating doses of endostatin until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose preceding that at which 2 of 6 patients experience dose limiting toxicity.
- interventionNames
- Biological: recombinant human endostatin
Primary outcomes (0)
[]Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
DISEASE CHARACTERISTICS: * Histologically proven advanced solid tumor for which no standard curative therapy exists * Must be amenable to biopsy At least 1 site of measurable disease outside of irradiated field * No brain metastases by CT or MRI scan PATIENT CHARACTERISTICS: * Age: 18 and over * Performance status: ECOG 0-1 * WBC greater than 3,000/mm3 * Absolute neutrophil count greater than 1,500/mm3 * Platelet count greater than 100,000/mm3 * Hemoglobin greater than 10 g/dL * Bilirubin less than 1.5 times upper limit of normal (ULN) * ALT and AST less than 2.0 times ULN * PT/PTT less than 1.5 times ULN * Creatinine less than 1.5 mg/dL OR creatinine clearance greater than 60 mL/min * Not pregnant or nursing * Negative pregnancy test * Fertile patients must use effective contraception * No concurrent uncontrolled medical or psychiatric disorder * No history of bleeding diathesis PRIOR CONCURRENT THERAPY: * No concurrent over the counter biologic agents (e.g., shark cartilage) * At least 3 weeks since prior chemotherapy (6 weeks since nitrosoureas or mitomycin) * No more than 3 prior chemotherapy regimens for metastatic or recurrent disease (ECOG 1) * Prior adjuvant chemotherapy for nonmetastatic disease allowed * Concurrent stable dose of hormone replacement therapy allowed * At least 3 weeks since prior radiotherapy * No concurrent radiotherapy * At least 24 hours since minor surgery (e.g., central venous placement) * At least 4 weeks since major surgery (e.g., laparotomy, thoracotomy, or craniotomy) * At least 30 days since other prior investigational agents * No concurrent herbal remedies * No concurrent usage of products containing heparin * No other concurrent anticancer therapy * Concurrent multivitamins allowed
References
Publications (0)
Data not yet available
No reference posted for this study.