Trial Information

Enlarged Prostate - A Phase III, double-blind, parallel-group, placebo-controlled clinical evaluation of NX-1207 for the treatment of BPH (Benign Prostatic Hyperplasia)

This study will evaluate the safety and efficacy of a 2.5mg dose of NX-1207 for the treatment of BPH (Benign Prostatic Hyperplasia). The study would last for 12 months from the start date of the trial. The study treatment would consist of an injection of NX-1207 or placebo into your prostate. If you receive placebo, you will be offered the opportunities to receive NX-1207 at the end of the study and to be followed for another 3 months.

Patient Inclusion Criteria:

Male aged 45 years and older
History of BPH for at least 1 year

Patient Exclusion Criteria:

Acute or chronic prostatitis in the past 12 months.
Documented urinary tract infection more than once in the past 12 months
Previous surgical or invasive prostate treatments such as TURP, TUMT, TUNA, laser, or any other minimally invasive treatment
History of use of self-catherization for urinary retention or urinary retention in the previous 12 months
History of prostate or bladder cancer
History of neurogenic bladder or lower urinary tract symptoms secondary to neurologic disease.

Nancy Manusov, Research Recruitment Specialist
Southeastern Research Group, Inc.
2000 Centre Pointe Boulevard
Tallahassee, FL 32308
Phone: 850-201-0411
Email: nmanusov@serginc.com

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Research Center Information: Southeastern Research Group, Inc.

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