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非在研适应症- |
最高研发阶段批准上市 |
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首次获批日期2008-05-01 |
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在研适应症- |
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最高研发阶段终止 |
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在研适应症- |
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最高研发阶段终止 |
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A multi centre, single-arm, prospective interventional study to evaluate the therapeutic effect of oral nutritional supplement on improving malnutrition and sarcopenia in chronic liver disease (CLD) patients.
A prospective, open label, single arm, multicenter, interventional, study to assess the efficacy and tolerability of early enteral nutrition in hospitalized patients
The Efficacy of T-regulatory Cell Depletion with E7777 Combined with Immune Checkpoint Inhibitor, Pembrolizumab, in Recurrent or Metastatic Solid Tumors: Phase I/II Study
Epithelial ovarian cancer (OC) is the most lethal gynecologic cancer: nearly 22,000 women are diagnosed with OC in the US annually and 63% are expected to die from their disease. The 5-year overall survival rate is unacceptably low at 20-30%, with > 50% of patients experiencing recurrence of their disease. Recurrent, platinum-resistant OC is characterized by a low response to chemotherapy (<10-15%) and poor prognosis, with overall survival estimated to be <12 months. Thus, there is an urgent need to identify novel therapies to improve outcomes for patients with recurrent, platinum resistant OC. The primary focus in this trial is targeting tumor associated immunosuppressive T-regs with E7777 combined with PD-1 inhibitor, pembrolizumab. This trial will enroll patients with solid tumors in the dose escalation portion and specified cohorts in the dose expansion portion. In the Phase I portion, 18-30 patients will be enrolled. In the dose expansion portion, approximately 40 patients (20 in each cohort) will be enrolled. Given the relatively poor prognosis and limited treatment options for these patients, this population is considered appropriate for trials of novel therapeutic candidates.
100 项与 Dr. Reddys Laboratories Tennessee LLC 相关的临床结果
0 项与 Dr. Reddys Laboratories Tennessee LLC 相关的专利(医药)
100 项与 Dr. Reddys Laboratories Tennessee LLC 相关的药物交易
100 项与 Dr. Reddys Laboratories Tennessee LLC 相关的转化医学