This is a randomized, double-blind, placebo-controlled study to evaluate the safety and tolerability of ENX-102 and determine a dose-response for the effects of ENX-102 in patients with GAD
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
38
Four weeks of ENX-102 (0.5, 1, or 3 mg) in capsule form followed by 2 weeks of tapered dose, taken orally once daily in the evening for a 6-week total treatment period
Six weeks of placebo in capsule form taken orally once daily in the evening for a 6-week total treatment period
MAC Clinical Research
Liverpool, UK, United Kingdom
MAC Clinical Research
Blackpool, United Kingdom
MAC Clinical Research
Manchester, United Kingdom
Safety and tolerability
• Incidence and severity of treatment-emergent AEs (TEAEs)
Time frame: 4 weeks
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