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Endostar Combination With Chemotherapy for the Metastatic Nasopharyngeal Carcinoma

U

University of Chinese Academy Sciences

Status and phase

Unknown
Phase 2

Conditions

Nasopharyngeal Carcinoma

Treatments

Drug: endostatin

Study type

Interventional

Funder types

Other

Identifiers

NCT01612286
ZhejaingCH-npc-02

Details and patient eligibility

About

The investigators designed this study to evaluate the efficiency and the acute toxicities of recombinant human endostatin (endostar) combined with chemotherapy in the metastatic nasopharyngeal carcinoma (NPC).

Full description

To evaluate the progression free survival (PFS), overall survival (OS), Acute adverse reaction of recombinant human endostatin (endostar) combined with chemotherapy to the metastatic nasopharyngeal carcinoma (NPC).

Enrollment

30 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diagnosed metastatic NPC patient who have received radiotherapy or chemoradiotherapy with an at least 6 months interval
  • Have measurable lesions
  • No dysfunction of the major organs
  • Can understand this study and give a signed informed consent certificates
  • without a history of allergic reaction to the biological agents

Exclusion criteria

  • Pregnant or lactating women; Women of child-bearing age without contraception
  • with a Serious infection or dysfunction of the major organs
  • have taken other antitumor drugs during the period of 30 days ahead of this clinical trial
  • allergic to the Escherichia coli preparations
  • Cann't understand this study and give a signed informed consent certificates

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

30 participants in 1 patient group

endostatin
Experimental group
Description:
chemotherapy concurrently with endostatin
Treatment:
Drug: endostatin

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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