TNF Blockade for Benign Prostatic Hyperplasia

Effects of TNF Blockade on Human BPH/LUTS

Recruiting Phase 2 Interventional Study
Benign Prostatic Hyperplasia (BPH)
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
45 – 80
Sex
Male
Trial phase
Phase 2
Study type
Interventional
Purpose
Basic Science
Participants needed
70 (estimated)
Sponsor
Endeavor Health · Other
Who this trial is looking for

This trial is looking for men aged 45 to 80 who have been diagnosed with benign prostatic hyperplasia (BPH). Participants will receive treatment and complete questionnaires about their condition.

Are You a Good Fit for This Trial?

You may be able to join if

  • I am male
  • I am between 45 and 80 years old
  • I have been diagnosed with BPH
  • My prostate volume is 60mL or more
  • My IPSS score is 8 or higher
  • I can complete questionnaires
  • I can provide informed consent
  • I can read, write, and speak in English

You may not be able to join if

  • I am female or intersex
  • I am under 45 or over 80 years old
  • I am a prisoner or detainee
  • I have urinary retention needing catheterization
  • I have gross hematuria
  • I have contraindications to adalimumab
  • I have autoimmune diseases
  • I have a history of lower urinary tract or pelvic malignancy

Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.

Think this trial could be right for you?

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Check Your Eligibility
About This Trial

Specific Aim 1. To evaluate the efficacy of TNF antagonist action in BPH/LUTS Specific Aim 2. Define the consequences of TNF antagonist therapy on prostate tissue Specific Aim 3. Identify genetic predictors to stratify patients with differential response to TNF-antagonist therapy.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Male sex * Age 45-80 years * Diagnosed by physician with BPH * Prostate volume ≥ 60mL * IPSS ≥ 8 * Able and willing to complete questionnaires * Able and willing to provide informed consent * Able to read, write, and speak in English * No prior treatment with TNF inhibitor (ad…
Contacts

Malgorzata Antoniak, Ph.D.

847-503-4282

MAntoniak@northshore.org

CONTACT

Pooja Talaty, MS MHA CCRP

847-503-4280

PTalaty@northshore.org

CONTACT