PG2 Injection for the Treatment of moderate-to Severe Fatigue in Breast Cancer Patients

NCT ID: NCT05440227

Last Updated: 2025-06-05

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE2
• Total Enrollment: 36 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-05-17
• Study Completion Date: 2026-06-30

Brief Summary

The objective of this study is to assess the efficacy of weekly PG2 regimen as a complementary treatment for patients with recurrent unresectable (local or regional) or metastatic breast cancer who experienced moderate to severe fatigue while receiving chemotherapies.

Detailed Description

The objective of this study is to assess the efficacy of weekly PG2 regimen as a complementary treatment for patients with recurrent unresectable (local or regional) or metastatic breast cancer who experienced moderate to severe fatigue while receiving chemotherapies. The primary endpoint is to examine whether PG2, compar ed with placebo, can successfully reduce patients' fatigue (observed via prorated area under the curve [AUC] for the Brief Fatigue Inventory [BFI] scores) when primed with PG2 for 8 weeks during their chemotherapy. The other efficacy endpoints including th e time course change of patient reported BFI, fatigue improvement response rate (fatigue improvement response is defined as those with at least 10% reduction from baseline in the total BFI scores) after 8 weeks, self perceived improvement, hematological improvement, health related quality of life, and safety profiles will also be assessed between treatment arms and compared with the baseline.

Conditions

Cancer-related Fatigue

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: TRIPLE

Study Groups

PG2 treatment group

500 mg PG2 injection will be administered to this group once per week for 8 weeks.

Group Type: EXPERIMENTAL

PG2 Lyo. Injection 500mg

Intervention Type: DRUG

PG2 Lyo. Injection 500mg (reconstituted with 0.9% normal saline 500ml) will be administered weekly for 8 weeks.

Placebo-controlled group

Placebo injection will be administered to this group once per week for 8 weeks.

Group Type: EXPERIMENTAL

Placebo 0.9% normal saline

Intervention Type: DRUG

0.9% normal saline 500ml will be administered weekly for 8 weeks.

Interventions

PG2 Lyo. Injection 500mg

PG2 Lyo. Injection 500mg (reconstituted with 0.9% normal saline 500ml) will be administered weekly for 8 weeks.

Intervention Type: DRUG

Placebo 0.9% normal saline

0.9% normal saline 500ml will be administered weekly for 8 weeks.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Women aged ≥ 20 years

2. ECOG performance score ≤ 2

3. Locally advanced, recurrent or metastatic, histologically documented breast cancer who is currently undergoing infusional chemotherapy regimen.

4. Presence of moderate to severe cancer related fatigue prior to randomization as defined by at least two records of usual fatigue score ≥ 4 on the numeric scale (0 -10), which must be ≥ 14 days apart.

5. Laboratory values obtained prior to randomization:

• Hgb ≥ 10 g/dL (patients must not be transfused ≤ 14 days to meet this criterion)
• Creatinine ≤ 1.2 x ULN
• AST (SGOT) or ALT (SGPT) ≤1.5 x ULN (or ≤5.0 x ULN for patients with liver metastases)

6. Pain under controlled of score ≤ 4 on the numeric scale (0 -10)

7. Life expectancy ≥ 3 months

8. Ability to complete patient questionnaires alone or with assistance.

9. Negative pregnancy test done ≤ 14 days prior to randomization, for women of childbearing potential only, and willing to take efficient contraceptives procedures to avoid pregnancy throughout the study period.

10. Willing to provide written informed consent and agree to follow the study requirements.

Exclusion Criteria

1. Known brain metastasis or primary CNS malignancy

2. Has known psychiatric or substance abuse disorders.

3. Malnutrition, active infection, uncontrolled thyroid disorder, uncontrollable hypertension or diabetes mellitus, significant pulmonary disease and cardiovascular disease.

4. Currently using any other pharmacologic agents.

5. Subject who is unwilling to receive transfusions when, at the investigator's discretion, it is required to control her anemia.

6. Other medical conditions that necessitate chronic systemic use of steroids (e.g. use of prednisolone > 10 mg daily or equivalent steroids fore more than 2 weeks).

7. ≤ 4 weeks from major surgery to randomization, including any procedure that requires general anesthetics.

8. Pain requiring opioid pain medication, however, over the counter analgesics such as acetaminophen or ibuprofen are allowed.

9. Use of monoamine oxidase inhibitors (MAOI) (such as Moclobemide).

10. Planning to start or complete any type of cancer therapy during the 8 weeks course of the study, once randomized on the study.

11. Use of any over the counter herbal/dietary supplement marketed for fatigue or energy.

12. Known history of hypersensitivity to Astragalus products.

13. Currently participating another interventional study or planning to join one in the upcoming 8 weeks after randomization.

14. Currently breast feeding.

15. With any other serious disease considered by the investigator not in the condition to enter into the trial.

• Minimum Eligible Age: 20 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

PhytoHealth Corporation

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Wei-Wu Chen, MD

Role: PRINCIPAL_INVESTIGATOR

National Taiwan University Hospital

Locations

National Taiwan University Hospital

Taipei, , Taiwan

Site Status: RECRUITING

Countries

Taiwan

Central Contacts

Tim Teng-Hsu Wang, PhD

Role: CONTACT

tim.wang@phytohealth.com.tw

+886 2 2545-3697 ext. 2317

Facility Contacts

Wei-Wu Chen, MD

Role: primary

Other Identifiers

PH-CP032

Identifier Type: -

Identifier Source: org_study_id