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A Study to Evaluate the Safety, Pharmacokinetics and Pharmacodynamics of ABBV-181 (Budigalimab) in Adult Participants With HIV-1

Home/A Study to Evaluate the Safety, Pharmacokinetics and Pharmacodynamics of ABBV-181 (Budigalimab) in Adult Participants With HIV-1
A Study to Evaluate the Safety, Pharmacokinetics and Pharmacodynamics of ABBV-181 (Budigalimab) in Adult Participants With HIV-1midwayadmin2020-05-15T15:18:14+00:00

A Study to Evaluate the Safety, Pharmacokinetics and Pharmacodynamics of ABBV-181 (Budigalimab) in Adult Participants With HIV-1

M19-939 · Trial ·

Major Inclusion/Exclusion Criteria:

  1. On current HIV medication for at least 12 weeks 
  2. HIV RNA <50 copies for 6 months
  3. CD4 >500 
  4. Willing to undergo ART interruption

 

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