Trial | NCT00813449  Report issue

Title

Safety Study of Combined Chemotherapy and Endostar to Untreated Patients With Advanced Melanoma
Multicenter, Double-blinding, Randomized Controlled, Phase II Clinical Trial on Combined Chemotherapy of Endostar (Recombinant Human Endostatin) for Untreated Patients With Advanced Melanoma

  • Phase

    Phase 2

  • Study Type

    Interventional

  • Status

    Unknown status

  • Intervention/Treatment

    endostatin dacarbazine ...

  • Study Participants

    140
Multicenter, double-blinding, randomized controlled, phase II clinical trial on combined chemotherapy of Endostar (Recombinant Human Endostatin) for untreated patients with advanced melanoma, To compare the efficacy and safety of Endostar combined with Dacarbazine and monotherapy of Dacarbazine for advanced melanoma
Dacarbazine (DTIC) has been approved for treating metastatic melanoma in the 1970s, and as a single agent gives a response rate of about 20%. There have been efforts to ameliorate this poor result by using DTIC in different combinations without a significant improvement. In addition, new studies with melanoma cells in vitro show that DTIC combination with Endostar, suggesting a potential clinical benefit from the concomitant treatment of DTIC and antiangiogenesis therapy. Endostar is a wild spectrum and safe antiangiogenesis factor which could suppress almost 65 kinds of tumor mass in animal models and affect about 12 percent human genome. The purpose of this study is to determine whether a combination therapy of endostar and DTIC is safe and can increase response rate and progression-free survival in patients (pts) with metastatic melanoma. We will evaluate the efficacy and safety of the Endostar plus DTIC and hope provide a new hope for the advanced melanoma patients.
Study Started
Aug 31
2008
Primary Completion
Aug 31
2010
Anticipated
Study Completion
Aug 31
2010
Anticipated
Last Update
Dec 08
2009
Estimate

Drug dacarbazine plus Endostar (Experimental group)

dacarbazine plus Endostar

  • Other names: dacarbazine plus Endostar

Drug dacarbazine plus placebo (control group)

dacarbazine plus placebo

  • Other names: dacarbazine plus placebo

A Experimental

Experimental group : Endostar combined with dacarbazine

2 Placebo Comparator

Control group : Dacarbazine combined with placebo

Criteria 

Inclusion Criteria:

Age > 18 years old, males or females;
Untreated patients with advanced melanoma confirmed by histopathology or cytology;
With tumor foci that can be evaluated by CT or MRI; at least one diameter ≥ 1 cm (including metastatic lymph nodes, diameter ≥ 1 cm confirmed by CT scan); or superficial focus ≥ 2 cm (confirmed by photos with calibration);
No contraindication for chemotherapy, with normal peripheral hemogram, renal and hepatic function: Peripheral hemogram: WBC≥4.0×109/L，PLT≥80×109/L，Hgb≥90g/L； Renal function: serum BUN and creatinine ≤2.5×UNL; Hepatic function: transaminase≤2.5×UNL, or ≤5×UNL in patients with liver metastasis;
Karnofsky performance scale≥70 (appendix 1); expected survival time≥3 months;
Patients are voluntary to participate and sign the informed contents.

Exclusion Criteria:

Pregnant or breast-feeding females; or females who have reproductive ability but do not take contraception method;
With severe acute infection uncontrolled; purulent or chronic infection with wounds difficult to recover;
With history of severe heart diseases, including congestive heart failure, uncontrolled arrhythmia with high risk, unstable angina pectoris, myocardial infarction, severe cardiac valvular diseases and refractory hypertension;
Have been treated by dacarbazine or dacarbazine included combination chemotherapy;
Patients with uncontrolled neurological, mental disease or psychosis, patients with poor compliance that cannot coordinate the therapy or describe the treatment response;
Uncontrolled brain metastasis patients with obvious manifestations of intracranial hypertension or neurological and mental disorders;
Allergic to any drug in the trial;
Patients with a second tumor;
Patients participating in other clinical trials;
Other conditions that are regarded for exclusion by the trialists
No Results Posted