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MechanismNMDA receptor antagonists |
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Inactive Indication- |
Drug Highest PhasePhase 1 |
First Approval Ctry. / Loc.- |
First Approval Date- |
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MechanismNMDA receptor antagonists |
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Inactive Indication- |
Drug Highest PhasePreclinical |
First Approval Ctry. / Loc.- |
First Approval Date- |
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MechanismAPOE antagonists |
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Inactive Indication- |
Drug Highest PhasePreclinical |
First Approval Ctry. / Loc.- |
First Approval Date- |
/ Not yet recruitingPhase 1 A Phase 1, Randomized, Double-blind, Placebo-controlled, Dose-escalation Study to Assess the Safety, Tolerability, and Pharmacokinetics of SP-101 Injection Following Single and Multiple Intravenous Doses in Healthy Adult Subjects
The goal of this First-In-Human (FIH) trial is to learn about safety, tolerability and pharmacokinetics of single and multiple ascending doses of SP-101 in healthy adult volunteers.
100 Clinical Results associated with Synphatec (Shanghai) Biopharmaceutical Technology Co., Ltd.
0 Patents (Medical) associated with Synphatec (Shanghai) Biopharmaceutical Technology Co., Ltd.
100 Deals associated with Synphatec (Shanghai) Biopharmaceutical Technology Co., Ltd.
100 Translational Medicine associated with Synphatec (Shanghai) Biopharmaceutical Technology Co., Ltd.