Last update 21 Nov 2024

SBK-001

Overview

Basic Info

Drug Type
Small molecule drug
Synonyms
Target
ACE2
Mechanism
ACE2 inhibitors(Angiotensin-converting enzyme 2 inhibitors)
Therapeutic Areas
Respiratory Diseases
Active Indication
Sputum excretion difficulty
Inactive Indication
Acute Lung Injury
Originator Organization
Chengdu Shibeikang Biomedical Technology Co Ltd
Active Organization
Chengdu Shibeikang Biomedical Technology Co Ltd
Inactive Organization-
Drug Highest PhasePhase 2
First Approval Date-
Regulation-
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Related

3
Clinical Trials associated with SBK-001
CTR20244096 / Not yet recruitingPhase 2
一项评估SBK001注射液在痰液黏稠、排痰困难的下呼吸道疾病患者中有效性和安全性的多中心、随机、双盲、安慰剂和阳性药平行对照的Ⅱ期临床研究
[Translation] A multicenter, randomized, double-blind, placebo- and active drug-controlled Phase II clinical study to evaluate the efficacy and safety of SBK001 injection in patients with lower respiratory tract diseases with thick sputum and difficulty expectorating
CTR20222019 / CompletedPhase 1
SBK001注射液多次给药在中国健康受试者中的 I 期耐受性、药代动力学研究。
[Translation] Phase I tolerability and pharmacokinetic study of multiple-dose SBK001 injection in healthy Chinese subjects.
CTR20220116 / CompletedPhase 1
SBK001注射液单次给药在中国健康受试者中的 I 期耐受性、药代动力学研究。
[Translation] Phase I tolerability and pharmacokinetic study of a single dose of SBK001 injection in healthy Chinese subjects.
100 Clinical Results associated with SBK-001
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100 Translational Medicine associated with SBK-001
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100 Patents (Medical) associated with SBK-001
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100 Deals associated with SBK-001
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R&D Status

10 top R&D records.
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IndicationHighest PhaseCountry/LocationOrganizationDate
Sputum excretion difficultyPhase 2
CN
Chengdu Shibeikang Biomedical Technology Co Ltd
04 Nov 2024
Acute Lung InjuryPhase 1
CN
Chengdu Shibeikang Biomedical Technology Co Ltd
16 Jan 2022
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date
CTR20222019 (Corporate Publications)
ManualManual
Phase 1
Acute Lung Injury
90
(qklmeaqzce) = 本品耐受性非常好，药代动力学呈现剂量依赖性 lieibeyecp (wxtcnqlxrr )
Positive
26 Aug 2022
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Approval

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Regulation

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