Clinical Trial

PG2 Breast Cancer Evaluation in Adjuvant Medicine-Survival Study

Study acronym: PG2 BEAM-S
Completed
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Summary
Astragalus polysaccharides (APS), acting as an immunomodulator, is known to modulate the tumor microenvironment and inhibit tumor growth and progression, thereby suggesting potential as an adjuvant cancer therapy to improve treatment outcomes. PG2 (APS Injection) has completed a clinical trial (Protocol name: PG2 Treatment for Reduction of Chemotherapy-Induced Toxicity and Encouraging Compliance with Chemotherapy among Stage II/III Breast Cancer Patients Receiving Adjuvant Chemotherapy , NCT03314805, hereinafter called the parent trial) aimed to show that PG2 treatment among stage II/III breast patients under adjuvant Epirubicin and cyclophosphamide (EC) regimen in reduction of chemotherapy-induced toxicities and encouraging compliance with chemotherapy. This study will further explore whether the addition of PG2 can delay cancer recurrence or metastasis, thereby conferring substantial survival benefits for early breast cancer patients with adjuvant chemotherapy by retrospectively collecting recurrence, metastasis, and survival information from patients enrolled in the parent trial.
Protocol Amendment History 4 changes
critical Trial completed 2026-07-03
notable Primary completion moved earlier: 2026-08-31 -> 2026-06-30 2026-07-03
minor Completion moved earlier: 2026-08-31 -> 2026-06-30 2026-07-03
critical Trial status changed: Not Yet Recruiting → Active, Not Recruiting 2026-05-30
Trial Details
NCT Number NCT07601113
Lead Sponsor Kun-Ming Rau
Conditions Survival
Enrollment 66 participants
Start Date 2026-05-27
Primary Completion 2026-06-30 (estimated)
Study Completion 2026-06-30 (estimated)
Updated on ClinicalTrials.gov 2026-07-06