Evaluate the Effects of GPI 1485 on Erectile Function Following Bilateral Nerve-Sparing Prostatectomy

Eisai

Status and phase

Completed

Phase 2

Conditions

Impotence

Prostate Cancer

Treatments

Drug: GPI 1485

Study type

Interventional

Funder types

Industry

Identifiers

NCT00090376

0501-0202

Details and patient eligibility

About

In this phase II study, an investigative (not approved by the FDA) drug called GPI 1485 is being assessed to see if it can help preserve erectile function after prostatectomy.

Full description

This drug has been tested in animals, and was shown to protect nerves from damage and to regrow damaged nerves in these animal studies. Participants will receive either GPI 1485 or a placebo (inactive pill). Participants will begin study medication 3 full days prior to their scheduled surgery.

GPI 1485 will be supplied as an oral tablet formulation to men who are candidates for bilateral nerve-sparing prostatectomies. Participants randomly assigned to receive GPI 1485 will be required to take four tablets four times a day by mouth.

GPI 1485 matching placebo will also be supplied as an oral tablet formulation. Participants randomly assigned to placebo will be required to take 4 placebo tablets four times a day by mouth.

Viagra® will be supplied as oral tablets beginning 1 month post-surgery. Patients can begin Viagra® 1 month post-surgery and may continue use until the end of the study, as needed.

The duration of this study is 12 months which includes 5 office visits to your doctor in addition to the surgery day. During this study you will also have other clinical evaluations including a physical exam, blood work, ECG (tracing of your heart rhythm) and urinalysis.

Participants enrolled in this study will also carry a handheld diary that is loaded with special protocol-specific software, which will be referred to as the patient experience diary (PED). Over the duration of this study, participants will complete their questionnaires and answer questions about their medication compliance in the electronic PED.

Sex

Male

Ages

40 to 69 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Clinical diagnosis of localized prostate carcinoma and scheduled to undergo curative surgical resection via bilateral nerve sparing procedure.
Localized prostate cancer is defined as:
- Gleason score <=7 (<=3 + <=4)
- PSA <=10 off of finasteride (Proscar®) and dutasteride (Avodart®)
- <=T2a stage disease
Motivated males, 40 to 69 years of age inclusive, and in the opinion of the investigator, are currently in a monogamous, sexually active relationship.
Males that have erectile function (EF) (without the use of pharmacotherapy within 30 days prior to screening assessment).
EF is defined as a score of >=26 on the EF domain of the IIEF questionnaire based on patient experiences over the 4 weeks prior to biopsy.
Body Mass Index (BMI) within the 18-34.9 kg/m2 range.
Able to swallow whole tablets equivalent to capsule size 0.
Available for protocol-specified visits and procedures.
Informed written consent must be provided prior to any study-specific procedures.

Exclusion criteria

Recent history, within 6 months before screening, of drug or alcohol abuse.
History of peripheral neuropathy.
History of acute or chronic depression that in the opinion of the investigator may interfere with protocol-specified efficacy measurements.
History of diabetes that requires use of insulin or oral hypoglycemic agents, myocardial infarction, or cerebrovascular accident.
History of spinal trauma or surgery to the brain or spinal cord.
Any medical disability or laboratory abnormality (e.g., serum creatinine > 2.0 mg/dL) that, in the opinion of the Investigator, may interfere with the protocol-specified safety and efficacy measurements, present an unacceptable risk to the patient's well-being, or compromise the patient's ability to provide informed consent.
History of pelvic radiation therapy (external beam radiation or brachytherapy).
Concomitant use of hormonal therapy, vasodilators (nitrates), dutasteride (Avodart®) or finasteride (Proscar®) within the 30 days prior to biopsy and throughout the study.
Concomitant use of therapeutic agents to treat ED other than those specified in the protocol is not permitted starting at least 30 days prior to biopsy and continuing throughout the study.
Previous exposure to GPI 1485 (previously AMG-474-00).
Treatment with an investigational agent within the 30 days before screening or scheduled to receive an investigational agent other than that specified by this protocol during the course of this study.
Any contraindication to Viagra® use
Unable to stop the use of inducers or inhibitors of cytochrome P450 (CYP) 3A4 from Baseline until the end of the study.