跳至主要内容
临床试验/EUCTR2004-005059-32-HU
EUCTR2004-005059-32-HU进行中(未招募)不适用

A Randomized, Double-Blind, Multicenter Study Comparing MDX-010 Monotherapy, MDX-010 in Combination with a Melanoma Peptide Vaccine, and Melanoma Peptide Vaccine Monotherapy in HLA-A*0201-Positive Patients with Previously Treated Unresectable Stage III or IV Melanoma - Not Available

Medarex, Inc.0 个研究点目标入组 1,051 人开始时间: 2006年2月16日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
Medarex, Inc.
入组人数
1,051

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Measureable Stage III or IV melanoma; at least 18 years of age; positive for HLA-A*0201; have demonstrated 1 of the following in response to at least 1 cycle of a first-line treatment with a single regimen containing IL-2, dacarbazine, and/or temozolamide: 1) relapse following an objective response 2) failed to demonstrate an objective response or 3) inability to tolerate treatment due to unacceptable toxicity; at least 4 weeks since treatment; negative pregnancy testing; life expectancy greater than 4 months; ECOG of 0 or 1; meet required lab values; and negative HIV, HepB and HepC tests.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Any other prior malignancy (except cured basal or squamous cell skin cancer, superficial bladder cancer, carcinoma in situ of the cervix); ocular melanoma; active, untreated CNS metastasis; prior treatment with the IMPs; prior treatment with any active autoimmune disease or a history of autoimmune disease except for patients with vitiligo; pregnant or nursing; concomitant therapy with IL-2, interferon or other non-study anti-melanoma immunotherapy regimens or other investigational therapies, or chronic use of systemic corticosteroids.

研究者

发起方
Medarex, Inc.

相似试验

进行中(未招募)
不适用
A Randomized, Double-Blind, Multicenter Study Comparing MDX-010 Monotherapy, MDX-010 in Combination with a Melanoma Peptide Vaccine, and Melanoma Peptide Vaccine Monotherapy in HLA-A*0201-Positive Patients with Previously Treated Unresectable Stage III or IV Melanoma - Not Available
EUCTR2004-005059-32-DEBristol-Myers Squibb International Corporation750
进行中(未招募)
不适用
A Randomized, Double-Blind, Multicenter Study Comparing MDX-010 Monotherapy, MDX-010 in Combination with a Melanoma Peptide Vaccine, and Melanoma Peptide Vaccine Monotherapy in HLA-A*0201-Positive Patients with Previously Treated Unresectable Stage III or IV Melanoma - Not AvailableHLA-A*0201-Positive Patients with Previously Treated, Unresectable Stage III or IV Melanoma
EUCTR2004-005059-32-BEBristol-Myers Squibb International Corporation750
进行中(未招募)
1 期
A Randomized, Double-Blind, Multicenter Study Comparing MDX-010 Monotherapy, MDX-010 in Combination with a Melanoma Peptide Vaccine, and Melanoma Peptide Vaccine Monotherapy in HLA-A*0201-Positive Patients with Previously Treated Unresectable Stage III or IV Melanoma - Not AvailableHLA-A*0201-Positive Patients with Previously Treated, Unresectable Stage III or IV Melanoma
EUCTR2004-005059-32-GBMedarex, Inc.750
已完成
3 期
A Randomized, Double-blind, Multicenter Study Comparing Magrolimab in Combination with Azacitidine versus Azacitidine Plus Placebo in Treatment-naïve Patients with Higher Risk Myelodysplastic Syndrome
NL-OMON52320Gilead Sciences14
进行中(未招募)
不适用
A Multicenter, Randomized, Double-Blind Study Comparing the Efficacy and Safety of Aflibercept Versus Placebo Administered Every 3 Weeks in Patients Treated with Docetaxel / Prednisone for Metastatic Androgen-Independent Prostate Cancer - VENICEPatients with metastatic androgen-independent prostate cancer
EUCTR2006-004756-20-DKsanofi-aventis recherche & développement1,200