WHO ICTRP trial

A multicenter, prospective, open, single-arm, Phase II clinical study exploring…

ChiCTR2300077760 · Chinese Clinical Trial Registry (ChiCTR) · Not Recruiting

Key facts

Trial ID ChiCTR2300077760
Public title A multicenter, prospective, open, single-arm, Phase II clinical study exploring gemcitabine in combination with oxaliplatin and eribulin (GOE) in relapsed refractory advanced male germ cell tumors
Scientific title A multicenter, prospective, open, single-arm, Phase II clinical study exploring gemcitabine in combination with oxaliplatin and eribulin (GOE) in relapsed refractory advanced male germ cell tumors
Primary sponsor Sun Yat-sen University Cancer Center
Registry Chinese Clinical Trial Registry (ChiCTR)
Recruitment status Not Recruiting
Study type Interventional study
Phase 2
Countries CHINA
Conditions Relapsed and refractory advanced male germ cell tumor
Interventions treatment group:Gemcitabine:800 mg/m2, ivgtt, d1, d8,every 3 weeks; Oxaliplatin:130mg/m2, ivgtt, d8,every 3 weeks; Eribulin:1.4mg/m2, ivgtt, d1, d8,every 3 weeks; PEG-GCSF:6mg,H,d9,every 3 weeks; Up to 6 courses or until disease progression…
Registration date Nov 18, 2023
Target size treatment group:43
Registry page chictr.org.cn

At a glance

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About WHO ICTRP trial registrations

The WHO ICTRP combines trial registrations from primary registries worldwide into a single searchable index. Contact and ethics-committee details are not shown here.

Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date:

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