TNF Blockade for Benign Prostatic Hyperplasia
Effects of TNF Blockade on Human BPH/LUTS
- Age
- 45 – 80
- Sex
- Male
- Trial phase
- Phase 2
- Study type
- Interventional
- Purpose
- Basic Science
- Participants needed
- 70 (estimated)
- Sponsor
- Endeavor Health · Other
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.
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?
Answer a few quick questions to see if you may meet the eligibility requirements.
Check Your EligibilitySpecific 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.
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