A Study to Evaluate the Pain Relieving Effects, Safety, and Tolerability of JNJ-42160443 for the Relief of Bladder Pain

This study is a randomized (study drug assigned by chance), double-blind (neither the
physician nor the patient knows the name of the assigned drug) study to evaluate the
analgesic efficacy, safety, and tolerability of JNJ-42160443 compared with placebo in
patients with moderate to severe, chronic bladder pain from Interstitial cystitis (IC)
and/or painful bladder syndrome (PBS). Interstitial cystitis (IC) and PBS are urological
disorders characterized by symptoms of bladder pain, urinary urgency, urinary frequency, and
the need to get up during the night in order to urinate. The study has 3 phases: a screening
phase (up to 3 weeks), a double-blind treatment phase (12 weeks), and a post-treatment phase
that ends 26 weeks after the last dose of study medication. The study duration will be
approximately 36 to 46 weeks.

A single dose of JNJ-42160443 (9 mg/ml) or matching placebo given as an injection under the
skin once every 4 weeks for up to 12 weeks.

Inclusion Criteria:

- Chronic pelvic pain (>6 months) perceived to be related to the urinary bladder and
accompanied by urinary symptoms such as frequent urination during the day and/or
night, and/or urgency to void

- Total score of 8 or greater on the O'Leary-Sant Interstitial Cystitis Symptom Index
(ICSI)

- The mean of the average pain intensity scores at screening phase >=5 (on a scale of 0
to 10)

- Medically stable

Exclusion Criteria:

- Urinary culture is positive for a urinary tract infection; Recent invasive therapy to
the bladder

- History or current conditions indicating that the bladder pain can be caused by
diagnoses other than IC/PBS (eg, pain caused by a confirmed or suspected neoplasm)

- History of malignancy within the past 2 years, with the exception of basal cell
carcinoma that has been successfully treated

- Women who are pregnant or breast-feeding

- A body mass index (BMI) of >39 kg/m2