|
|
|
|
|
Inactive Indication- |
Drug Highest PhasePhase 2 |
First Approval Ctry. / Loc.- |
First Approval Date- |
|
MechanismHBsAg inhibitors |
|
|
|
Inactive Indication- |
Drug Highest PhasePhase 1 |
First Approval Ctry. / Loc.- |
First Approval Date- |
Target- |
Mechanism- |
|
|
|
Inactive Indication- |
Drug Highest PhasePreclinical |
First Approval Ctry. / Loc.- |
First Approval Date- |
HT-101注射液或HT-102注射液在慢性乙肝病毒感染患者中多次给药的安全性、耐受性、药代动力学及药效动力学研究
[Translation] Safety, tolerability, pharmacokinetics and pharmacodynamics of HT-101 injection or HT-102 injection after multiple administration in patients with chronic hepatitis B virus infection
研究慢性乙肝病毒感染患者多次皮下注射HT-101注射液或HT-102注射液的安全性及耐受性
[Translation] To study the safety and tolerability of multiple subcutaneous injections of HT-101 injection or HT-102 injection in patients with chronic hepatitis B virus infection
Safety, Tolerability, Pharmacokinetic and Pharmacodynamic Characteristics of HT-102Injection in Healthy Subjects and Hepatitis B E Antigen-Negative Patients with Chronic Hepatitis B Virus Infection: a Randomized, Double-blind, Placebo-controlled, Single and Multiple Subcutaneous Injections, and Dose Escalation Phase 1 Clinical Study
Safety, Tolerability, Pharmacokinetic and Pharmacodynamic Characteristics of HT-102 (BM012) Injection in Healthy Subjects and Hepatitis B e Antigen-Negative Patients with Chronic Hepatitis B Virus Infection: A Randomized, Double-blind, Placebo-controlled, Single and Multiple Subcutaneous Injections, and Dose Escalation Phase 1 Clinical Study
Safety, Tolerability, Pharmacokinetic and Pharmacodynamic Characteristics of HT-101 Injection in Healthy Subjects and Patients with Chronic Hepatitis B Virus Infection: a Randomized, Double-blind, Placebo-controlled, Single and Multiple Doses, and Dose Escalation Phase 1 Clinical Study
Phase 1 Study of HT-101 in Healthy Subjects and Patients With Chronic Hepatitis B The trial consisted of two components. Part A involved a single ascending dose study where healthy participants were administered one dose of HT-101 or placebo subcutaneously (SC). Part B involved a multiple ascending dose study where participants with chronic hepatitis B virus infection were administered two dose of HT-101 or placebo every 4 weeks subcutaneously (SC).
100 Clinical Results associated with Suzhou Xingyao Kunze Biopharmaceutical Co., Ltd.
0 Patents (Medical) associated with Suzhou Xingyao Kunze Biopharmaceutical Co., Ltd.
100 Deals associated with Suzhou Xingyao Kunze Biopharmaceutical Co., Ltd.
100 Translational Medicine associated with Suzhou Xingyao Kunze Biopharmaceutical Co., Ltd.