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Donafenib Monotherapy for Previously Treated Metastatic Gastric Cancer

Primary Purpose

Gastric Cancer

Status
Terminated
Phase
Phase 1
Locations
China
Study Type
Interventional
Intervention
donafenib tosilate tablets
Sponsored by
Suzhou Zelgen Biopharmaceuticals Co.,Ltd
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Gastric Cancer focused on measuring donafenib

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • All patients provided written, informed consent.
  • Have histological or cytological documentation of gastric adenocarcinoma;
  • Have received currently approved standard therapies and to have disease progression during or within 3 months after the last administration of the last standard therapy or to have stopped standard therapy because of unacceptable toxic effects.
  • Standard therapies include as many of the following as were licensed: a fluoropyrimidine,oxaliplatin,irinotecan, paclitaxel,docetaxel;and trastuzumab for patients who had Her-2 positive tumours;
  • Have an Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1;
  • Life expectancy of at least 3 months;
  • Have adequate bone-marrow, liver, and renal function at the start of the trial.
  • Prothrombin time international normalized ratio≤1.5;

Exclusion Criteria:

  • Patients with brain metastases.
  • Patients receiving cytotoxic chemotherapy, immunotherapy or hormonal therapy, radiotherapy to site of measurable or evaluable disease within the previous 4 weeks.
  • Patients had evidence of clinically active interstitial lung disease or abnormal blood results by predefined criteria (serum bilirubin >1.5 times upper limit of reference range, aspartate or alanine aminotransferase>2.5 times the upper limit of normal if no demonstrable liver disease).

Sites / Locations

  • The Affiliated Hospital of Nanjing University Medical School
  • Affiliated Cancer Center of Academy of Military Medical Sciences

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

donafenib tosilate tablets

Arm Description

200mg bid

Outcomes

Primary Outcome Measures

Number of Participants with Adverse Events
patients with adverse events/all patients*100%

Secondary Outcome Measures

Tumor response
complete response and partial response patients/all patients*100%
Progression-free survival time
median progress-free survival time

Full Information

First Posted
June 25, 2015
Last Updated
May 4, 2023
Sponsor
Suzhou Zelgen Biopharmaceuticals Co.,Ltd
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1. Study Identification

Unique Protocol Identification Number
NCT02489214
Brief Title
Donafenib Monotherapy for Previously Treated Metastatic Gastric Cancer
Official Title
A Phase 1B Study of Donafenib Monotherapy for Previously Treated Metastatic Gastric Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
November 2022
Overall Recruitment Status
Terminated
Why Stopped
Corporate policy adjustments
Study Start Date
May 16, 2016 (Actual)
Primary Completion Date
June 13, 2019 (Actual)
Study Completion Date
June 13, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Suzhou Zelgen Biopharmaceuticals Co.,Ltd

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This open-label, one-center, noncomparative, two-stage phase 1B trial assessed the donafenib in advanced gastric cancer.
Detailed Description
This open-label, one-center, noncomparative, two-stage phase 1B trial assessed the tyrosine kinase inhibitor donafenib tosilate tablets (400 mg/d,200mg bid) in patients with advanced, inoperable gastric cancer progressing after chemotherapy . The primary endpoint is the safety.The secondary endpoints are tumor response and progression-free survival time.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gastric Cancer
Keywords
donafenib

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
13 (Actual)

8. Arms, Groups, and Interventions

Arm Title
donafenib tosilate tablets
Arm Type
Experimental
Arm Description
200mg bid
Intervention Type
Drug
Intervention Name(s)
donafenib tosilate tablets
Other Intervention Name(s)
CM4307
Intervention Description
200mg bid
Primary Outcome Measure Information:
Title
Number of Participants with Adverse Events
Description
patients with adverse events/all patients*100%
Time Frame
54 weeks
Secondary Outcome Measure Information:
Title
Tumor response
Description
complete response and partial response patients/all patients*100%
Time Frame
54 weeks
Title
Progression-free survival time
Description
median progress-free survival time
Time Frame
54 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All patients provided written, informed consent. Have histological or cytological documentation of gastric adenocarcinoma; Have received currently approved standard therapies and to have disease progression during or within 3 months after the last administration of the last standard therapy or to have stopped standard therapy because of unacceptable toxic effects. Standard therapies include as many of the following as were licensed: a fluoropyrimidine,oxaliplatin,irinotecan, paclitaxel,docetaxel;and trastuzumab for patients who had Her-2 positive tumours; Have an Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1; Life expectancy of at least 3 months; Have adequate bone-marrow, liver, and renal function at the start of the trial. Prothrombin time international normalized ratio≤1.5; Exclusion Criteria: Patients with brain metastases. Patients receiving cytotoxic chemotherapy, immunotherapy or hormonal therapy, radiotherapy to site of measurable or evaluable disease within the previous 4 weeks. Patients had evidence of clinically active interstitial lung disease or abnormal blood results by predefined criteria (serum bilirubin >1.5 times upper limit of reference range, aspartate or alanine aminotransferase>2.5 times the upper limit of normal if no demonstrable liver disease).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bao Rui, Doctor
Organizational Affiliation
The affiliated hospital of Nanjing University Medical School
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Affiliated Hospital of Nanjing University Medical School
City
Nanjing
State/Province
Jiangsu
ZIP/Postal Code
210008
Country
China
Facility Name
Affiliated Cancer Center of Academy of Military Medical Sciences
City
Beijing
ZIP/Postal Code
100071
Country
China

12. IPD Sharing Statement

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Donafenib Monotherapy for Previously Treated Metastatic Gastric Cancer

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