Thymosin-α1 in Cancer-Related Fatigue

Sponsor
Zhigang Zhang (Other)
Overall Status
Unknown status
CT.gov ID
NCT02127268
Collaborator
(none)
200
1
2
80
2.5

Study Details

Study Description

Brief Summary

Cancer-related fatigue (CRF) is a distressing, persistent, subjective sense of physical, emotional, and/or cognitive tiredness or exhaustion related to cancer or cancer treatment that is not proportion to recent activity and interferes with usual functioning. Compared with general fatigue, CRF have the characteristics of long duration and generally cannot alleviate by rest or sleep, serious impact on the patient's work, study, entertainment and family life, and thus greatly affect the recovery, self-care ability and life quality of patients. Many dates showed that 70%~100% of cancer patients experienced cancer-related fatigue.For cancer-related fatigue there is no good treatment and intervention, in recent years, many clinical trials are carried out; central nervous stimulant, such as methylphenidate; acupuncture, aerobic exercise. All those measures may have certain therapeutic effect for CRF, but don't have exact evidences from massive RCT to confirm.

Thymosin-α1 (T-α1), a synthetic 28-amino acid peptide with multiple biological activities primarily directed towards immune response enhancement, this drug is used for the treatment of HBV and hepatitis C virus (HCV) infections, and being developed for the treatment of non-small cell lung cancer (NSCLC), hepatocellular carcinoma, AIDS and malignant melanoma. T-α1 is able to potentiate the action of cytokines and also reduce the hematological toxicity of cytotoxic drug therapy, such as cyclophosphamide, 5-fluorouracil, dacarbazine.

In this studies, we want to demonstrated that the effectiveness of Thymosin-α1 for cancer-related fatigue in cancer patients who undergo chemotherapy.

Condition or Disease Intervention/Treatment Phase
Phase 3

Study Design

Study Type:
Interventional
Anticipated Enrollment :
200 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Treatment
Official Title:
Thymosin-α1 for Cancer-Related Fatigue in Cancer Patients Who Undergo Chemotherapy: A Randomized Controlled Trial
Actual Study Start Date :
Apr 1, 2014
Anticipated Primary Completion Date :
Apr 1, 2020
Anticipated Study Completion Date :
Dec 1, 2020

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Arm T

Will be treated with Thymosin-α1 1.6mg twice a week from day 1 of chemotherapy

Drug: Thymosin-α1
with Thymosin-α1 1.6mg twice a week

No Intervention: Arm B

With best support according to NCCN Guideline

Outcome Measures

Primary Outcome Measures

  1. Change in Cancer-Related Fatigue Scale [baseline and 4 weeks]

Secondary Outcome Measures

  1. improvement in Quality of Life [baseline and 4 weeks]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Men and women aged 18 years and older.

  2. The life expectancy at least 6 months.

  3. With a definite pathological diagnosis of cancer, and undergo chemotherapy.

  4. Patients who are willing to participate in the study.

Exclusion Criteria:
  1. Thymosin-α1 allergy.

  2. Using the spirit excitement or stimulant drugs.

  3. With brain metastasis or primary malignant brain tumors.

  4. With mental disorders, such as suffering from dementia, delirium, obsessive-compulsive disorder, schizophrenia, epilepsy.

  5. Other specific causes of fatigue: such as anemia, thyroid function is low, insomnia, uncontrolled pain.

  6. Serious HRS cardiopulmonary function disorder.

  7. Women during pregnancy and lactation.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Cancer institute Hangzhou Zhejiang China 310009

Sponsors and Collaborators

  • Zhigang Zhang

Investigators

  • Study Director: Jian Huang, Doctor, Zhejiang University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Zhigang Zhang, Doctor, Zhejiang University
ClinicalTrials.gov Identifier:
NCT02127268
Other Study ID Numbers:
  • T-CRF
First Posted:
Apr 30, 2014
Last Update Posted:
Apr 10, 2019
Last Verified:
Apr 1, 2019
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 10, 2019