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在研机构- |
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最高研发阶段无进展 |
首次获批国家/地区- |
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A Sequential-Cohort, Double-Blind, Placebo-Controlled, Multiple Ascending Oral Dose Study of the Safety and Pharmacokinetics of BTA-C585 in Healthy Volunteers
This is a single center, sequential-cohort, double-blind, placebo-controlled, multiple ascending dose (MAD), 7-day treatment period study in healthy subjects.
A Double-Blind, Placebo-Controlled, Single Ascending Oral Dose Study of the Safety and Pharmacokinetics of BTA-C585 in Healthy Volunteers
This is a placebo-controlled, double-blind, randomized, single dose escalation Phase 1 clinical trial to determine the safety and tolerability of BTA-C585 administered orally to healthy subjects.
A Phase 2, Multicenter, Randomized, Double-blind, Placebo-controlled Dose-ranging Study of Vapendavir in Moderate to Severe Asthmatic Adults with Symptomatic Human Rhinovirus Infection. - Phase 2 Asthma
100 项与 Biota Pharmaceuticals, Inc. /Antibiotics Assets/ 相关的临床结果
0 项与 Biota Pharmaceuticals, Inc. /Antibiotics Assets/ 相关的专利(医药)
100 项与 Biota Pharmaceuticals, Inc. /Antibiotics Assets/ 相关的药物交易
100 项与 Biota Pharmaceuticals, Inc. /Antibiotics Assets/ 相关的转化医学