Safety and Efficacy of Kanglaite Gelcaps in Prostate Cancer

Stopped early · Phase 2

Conditions studied: Prostate Cancer

In brief

This research is being done to evaluate the safety and efficacy of the investigational Kanglaite gelcap (KLTc) on PSA in men with prostate cancer when given for twelve months.

Key facts

Study ID

NCT01483586

Run by

KangLaiTe USA

People needed

90

Starts

2011-11-01

Expected to finish

2013-12-01

Last updated by the study team

2014-04-14

Who can join

Age: 18 and older. Sex: male. Healthy volunteers: not accepted.

You may qualify if…

• confirmed adenocarcinoma of the prostate
• undergone definitive treatment (surgery, surgery with radiation therapy, cryotherapy, radiation therapy or brachytherapy) for the primary prostate tumor with a rising PSA
• life expectancy greater than 6 months
• has Eastern Cooperative Oncology Group (ECOG) performance status 0, 1, or 2
• use of other dietary/herbal supplements (e.g. saw palmetto, selenium, etc.) has been stable for at least 2 months prior to screening and the patient agrees not to stop or change the dose while participating in the study.
• Adequate hepatic function with serum bilirubin ≤ 1.5 times the upper institutional limits of normal, ALT and AST ≤ 2.5 times the upper institutional limits of normal
• Adequate renal function with serum creatinine ≤ 1.5 times the upper institutional limits of normal
• Adequate hematologic function (absolute neutrophil counts ≥ 1,500 mm3 and platelets ≥ 100,000 mm3)
• All electrolytes (including potassium, sodium, and serum or ionized calcium) must be within normal limits

You may not qualify if…

• Patients with evidence of metastatic disease would be excluded, except for presence of positive lymph nodes from the surgical pathology. Similarly, patients with radiological evidence of lymph nodes < 2 cm that lack pathological confirmation would be eligible
• Patients with a PSA doubling time of <6months at screening would be excluded
• Patients meeting Phoenix criteria for biochemical failure (nadir + ≥2ng/mL increase in serum PSA) who wish additional conventional therapy
• Any concurrent malignancy other than adequately treated basal or squamous cell skin cancer or superficial bladder cancer
• Any psychiatric or other disorders such as dementia that would prohibit the patient from understanding or rendering informed consent or from fully complying with protocol treatment and follow-up
• Inability to swallow capsules
• Patients with a known history of gastrointestinal disease, surgery or malabsorption that could potentially impact the absorption of the study drug
• Patients requiring the use of a feeding tube
• Receipt of prior chemotherapy

Where it is running

• Northwestern University — Chicago, Illinois, United States
• North Shore University — Evanston, Illinois, United States
• Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins — Baltimore, Maryland, United States
• The Cancer Institute of New Jersey — New Brunswick, New Jersey, United States
• Duke University — Durham, North Carolina, United States

Full record on ClinicalTrials.gov

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