Last update 21 Dec 2024
SGB-9768
Last update 21 Dec 2024
Overview
Basic Info
Drug Type siRNA |
Synonyms SGB 9768 |
Target |
Mechanism C3 inhibitors(Complement C3 inhibitors) |
Therapeutic Areas |
Active Indication |
Inactive Indication- |
Originator Organization |
Active Organization |
Inactive Organization- |
Drug Highest PhasePhase 1 |
First Approval Date- |
Regulation- |
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Related
3
Clinical Trials associated with SGB-9768在中国健康受试者中评价单次皮下给药SGB-9768注射液的安全性、耐受性、药代动力学以及药效学特征的I期临床试验
[Translation] A Phase I clinical trial to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics of a single subcutaneous dose of SGB-9768 injection in healthy Chinese subjects
A Phase 1, Randomized, Double-blind, Placebo-controlled Single Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Subcutaneously Administered SGB-9768 in Healthy Volunteers
A Phase 1, Randomized, Double-blind, Placebo-Controlled Single Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Subcutaneously Administered SGB-9768 in Healthy Volunteers
100 Clinical Results associated with SGB-9768
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100 Translational Medicine associated with SGB-9768
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100 Patents (Medical) associated with SGB-9768
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100 Deals associated with SGB-9768
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R&D Status
10 top R&D records. to view more data
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| Indication | Highest Phase | Country/Location | Organization | Date |
|---|---|---|---|---|
| C3 glomerulopathy | Phase 1 | CN | 18 Jul 2024 | |
| Glomerulonephritis, IGA | Phase 1 | CN | 18 Jul 2024 | |
| Glomerulonephritis, Membranoproliferative | Phase 1 | CN | 18 Jul 2024 | |
| Immune System Diseases | IND Approval | NZ | 27 Feb 2024 |
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Clinical Result
Clinical Result
Indication
Phase
Evaluation
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NCT06501573 (NEWS) Manual  | Phase 1 | - | 55 | kwcvlnjagu(amvdmdmzck) = SGB-9768表现出良好的安全性和耐受性。 xtltzgdynf (ignxhzyebq ) View more | Positive | 11 Dec 2024 | |
Placebo |
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