Actively Recruiting

Age: 18Years - 70Years
All Genders
NCT07096479

Telpegfilgrastim Injection to Reduce the Risk of Neutropenia in Patients With Solid Tumor

Led by Anhui Provincial Hospital · Updated on 2025-07-31

318

Participants Needed

2

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The objective of this real world study is to confirm the efficacy and saftey of Telpegfilgrastim injection for the prevention of chemotherapy-induced Neutropenia in Patients With Malignant solid tumor.

CONDITIONS

Official Title

Telpegfilgrastim Injection to Reduce the Risk of Neutropenia in Patients With Solid Tumor

Who Can Participate

Age: 18Years - 70Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Male or female aged 18 to less than 70 years
  • Body weight of at least 45 kg
  • Histologically or cytologically confirmed malignant solid tumor
  • Receiving a 3-week chemotherapy regimen with high risk of febrile neutropenia or moderate risk with increased neutropenia risk factors
  • Karnofsky Performance Scale score of 70 or higher
  • White blood cell count at least 3.5 �d7 10 9/L and absolute neutrophil count at least 1.5 �d7 10 9/L before chemotherapy
  • Life expectancy of at least 6 months
  • Willingness to comply with study protocol and provide written informed consent
Not Eligible

You will not qualify if you...

  • Received any other PEG-rhG-CSF within 4 weeks before the study
  • Receiving intermittent or continuous chemotherapy such as albumin paclitaxel or capecitabine
  • Previous or expected radiation therapy to more than 25% of total bone marrow
  • Significant organ dysfunction including liver function (ALT, TBil) >2.5 times upper limit of normal or >5 times if liver metastasis present; hepatitis B or C infection or cirrhosis; renal function (creatinine) >1.5 times upper limit of normal
  • Pregnant or breastfeeding women
  • Hypersensitivity to rhG-CSF or other biological agents
  • Any other conditions judged by investigators to affect study progress or results

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

Anhui province hospital

Hefei, Anhui, China, 230000

Actively Recruiting

2

Anhui province hospital

Hefei, Anhui, China, 230000

Actively Recruiting

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How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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