HIV Infections Clinical Trial
Official title:
A Multicenter, Randomized, Double-Blinded, Dose-Escalation Study Evaluating the Safety and Antiretroviral Activity of HBY 097 Versus HBY 097 Plus AZT in Patients With Asymptomatic or Mildly Symptomatic HIV Infection
To obtain preliminary information on the safety, tolerability, and antiretroviral activity
of HBY 097 alone or in combination with zidovudine ( AZT ) versus AZT alone.
PER 1/19/96 AMENDMENT: AZT monotherapy arm was eliminated.
Patients are randomized to receive one of three doses of HBY 097 with or without AZT or AZT
alone for 12 weeks (AZT monotherapy arm eliminated per 1/19/96 amendment). All patients at a
given dose level of HBY 097 must be enrolled and adequate safety data obtained before
escalation in subsequent patients begins. Additional patients are entered at the optimal
dose of HBY 097. Patients are evaluated weekly for the first 4 weeks and then every 2 weeks
for the next 9 weeks.
PER AMENDMENT: Enrollment to the lowest dose cohort is completed.
;
Endpoint Classification: Safety Study, Masking: Double-Blind, Primary Purpose: Treatment
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