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Sodium Thiosulfate

Generic Name
Sodium Thiosulfate
Brand Names
Pedmarqsi

Overview

No overview information available.

Background

No background information available.

Indication

⑴治疗氰化物中毒,与高铁血红蛋白形成剂联合应用; ⑵治疗降压药硝普钠过量中毒; ⑶治疗可溶性钡盐(如硝酸钡)中毒; ⑷治疗砷、汞、铋、铅等金属中毒,但首选二巯基类药物及依地酸类药物; ⑸作为非特异性抗炎药,用于皮炎、湿疹、荨麻疹、药物性皮炎、副银屑病的治疗【1.《糖皮质激素类药物临床应用指导原则》;2.《中西医结合系统药物治疗湿疹皮炎类皮肤病专家共识》2015;3.《临床诊疗指南皮肤病与性病分册》】。

Associated Conditions

No associated conditions information available.

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor
2024/03/01
Not Applicable
Not yet recruiting
Alp Sener
2023/03/06
Early Phase 1
Suspended
2022/05/19
Phase 3
Recruiting
2021/08/24
Phase 3
Recruiting
2021/04/15
Phase 1
Recruiting
2020/09/09
Phase 2
Completed
Hyunseok Kang, MD
2020/07/20
Phase 3
Recruiting
Shanghai Children's Medical Center
2020/02/10
Phase 1
Completed
Decibel Therapeutics
2020/02/05
Phase 2
UNKNOWN
Soraia Azevedo
2019/12/30
Early Phase 1
Terminated

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
Fennec Pharmaceuticals Inc.
73077-010
INTRAVENOUS
12.5 g in 100 mL
9/30/2022
Hope Pharmaceuticals
60267-705
INTRAVENOUS
250 mg in 1 mL
11/16/2023

HSA Drug Approvals

Approved Product
Manufacturer
Approval Number
Dosage Form
Strength
Approval Date
No HSA approvals found for this drug.

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
Sodium Thiosulfate for Injection
国药准字H31020533
化学药品
注射剂
5/22/2020
Sodium Thiosulfate for Injection
国药准字H31020534
化学药品
注射剂
5/22/2020
Sodium Thiosulfate Injection
国药准字H11020020
化学药品
注射剂(小容量注射剂)
9/23/2021
Sodium Thiosulfate Injection
国药准字H12020993
化学药品
注射剂
7/27/2020
Sodium Thiosulfate Injection
国药准字H20233614
化学药品
注射剂
12/18/2023
Sodium Thiosulfate Injection
国药准字H50020770
化学药品
注射剂
9/30/2020
Sodium Thiosulfate Injection
国药准字H20233615
化学药品
注射剂
12/18/2023
Sodium Thiosulfate Injection
国药准字H50020771
化学药品
注射剂
9/30/2020
Sodium Thiosulfate Injection
国药准字H50020769
化学药品
注射剂
9/30/2020
Sodium Thiosulfate Injection
国药准字H20254180
化学药品
注射剂
5/13/2025

PPB Drug Approvals

Approved Product
Registration No.
Company
Licence No.
Strength
Registration Date
No PPB approvals found for this drug.

TGA Drug Approvals

Approved Product
ARTG ID
Sponsor
Registration Type
Status
Registration Date
No TGA approvals found for this drug.
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