Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT02985333

Paclitaxel,Cyclophosphamide and Dexamethasone for Relapsed or Refractory Multiple Myeloma

Efficacy and Safety of Paclitaxel/Cyclophosphamide/Dexamethasone to Treat Patients With Relapsed or Refractory Multiple MyelomaRefractory

Status
Withdrawn
Phase
Phase 2
Study type
Interventional
Enrollment
0 (actual)
Sponsor
Sun Yat-sen University · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate the efficacy and safety of paclitaxel in combination with cyclophosphamide and dexamethasone in chinese patients with relapsed/refractory multiple myeloma.

Detailed description

Treatment for relapsed/refractory multiple myeloma (MM)remains a crucial challenge.The investigators have previously shown that the combination of paclitaxel and cyclophosphamide acts synergistically to induce apoptosis of myeloma cells in vitro. Based on these preclinical studies, the investigators initiated a phase II clinical trial of paclitaxel 175 mg/m(2) IV over 3 h d1 combined with cyclophosphamide 200 mg/m(2) IV over 30-60 min d1,3,5 and dexamethasone 20mg IV over 30-60 min d1-4 in patients with relapsed or refractory MM. This regimen was administered every four weeks for a total of six cycles

Conditions

Interventions

TypeNameDescription
DRUGPaclitaxelPaclitaxel 170 mg/m(2) IV over 3 h d1
DRUGCyclophosphamideCyclophosphamide 200mgmg/m(2) IV d1,3,5
DRUGDexamethasoneDexamethasone 20mg iv d1-4

Timeline

Start date
2014-01-01
Primary completion
2018-12-01
Completion
2019-06-01
First posted
2016-12-07
Last updated
2018-05-14

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT02985333. Inclusion in this directory is not an endorsement.