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Gemcitabine Combined With Endostar and Envafolimab in Elderly Patients With Locally Advanced Nasopharyngeal Carcinoma

U

University of Chinese Academy Sciences

Status and phase

Enrolling
Phase 2

Conditions

Nasopharyngeal Carcinoma

Treatments

Drug: Endostar and Envafolimab

Study type

Interventional

Funder types

Other

Identifiers

NCT06055816
GEE study

Details and patient eligibility

About

Gemcitabine Combined With Endostar and Envafolimab in Elderly Patients With Locally Advanced Nasopharyngeal Carcinoma

Enrollment

40 estimated patients

Sex

All

Ages

65+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Aged ≥65 years with newly pathologically confirmed NPC
  • Karnofsky performance status ≥60
  • Clinical stage III-IVA (Union for International Cancer Control and American Joint Committee on Cancer staging system for NPC, 8th edition)
  • Adequate organ function

Exclusion criteria

  • Cancer history
  • Prior radiotherapy, cytotoxic chemotherapy, immunotherapy or target therapy
  • Life-expectance within 6 months

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

40 participants in 1 patient group

Gemcitabine Combined With Endostar and Envafolimab
Experimental group
Description:
Neoadjuvant therapy consisting of gemcitabine (1000mg/m2 d1,8) , endostar (150mg 3-day continuous infusion) and envafolimab (240mg d1) was given every 3 weeks for 3 cycles. Endostar, administered every 3 weeks (150mg 3-day continuous infusion), was given concurrently with intensity-modulated radiotherapy.
Treatment:
Drug: Endostar and Envafolimab

Trial contacts and locations

1

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Central trial contact

Xiaozhong Chen

Data sourced from clinicaltrials.gov

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