Last update 24 Sep 2026

RAB-202

Overview

Basic Info

Drug Type
Synthetic peptide
Synonyms
4-(2-Methylanilidocarbamoyl)-phenylacetyl-L-Citrullyl-L-Glutamyl-L-Seryl-L-Valyl-2-[2-(2-aminoethoxy)ethoxy]acetyl-N6-[N-(19-carboxy-1-oxononadecyl)-L-gamma-glutamyl]-L-Lysyl amide, RAB202
Target-
Action-
Mechanism-
Therapeutic Areas
Congenital DisordersEndocrinology and Metabolic DiseaseSkin and Musculoskeletal Diseases+ [1]
Active Indication
Osteogenesis ImperfectaOsteoporosisSpinal fusion
Inactive Indication-
Originator Organization
Zhongshan Lebo Ruichen Biopharmaceutical Co Ltd.Zhongshan Lebo Ruichen Biopharmaceutical Co Ltd.
Active Organization
Zhongshan Lebo Ruichen Biopharmaceutical Co Ltd.Zhongshan Lebo Ruichen Biopharmaceutical Co Ltd.
Inactive Organization-
License Organization-
Drug Highest PhasePreclinical
First Approval Date-
RegulationOrphan Drug (United States), Rare Pediatric Disease (United States)

Related

100 Clinical Results associated with RAB-202
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100 Translational Medicine associated with RAB-202
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100 Patents (Medical) associated with RAB-202
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100 Deals associated with RAB-202
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R&D Status

10 top R&D records.
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IndicationHighest PhaseCountry/LocationOrganizationDate
Osteogenesis ImperfectaPreclinical
United States
Zhongshan Lebo Ruichen Biopharmaceutical Co Ltd.Zhongshan Lebo Ruichen Biopharmaceutical Co Ltd.
17 Sep 2026
OsteoporosisPreclinical
China
Zhongshan Lebo Ruichen Biopharmaceutical Co Ltd.Zhongshan Lebo Ruichen Biopharmaceutical Co Ltd.
04 Jun 2025
Spinal fusionPreclinical
China
Zhongshan Lebo Ruichen Biopharmaceutical Co Ltd.Zhongshan Lebo Ruichen Biopharmaceutical Co Ltd.
04 Jun 2025
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Clinical Result

Indication
Phase
Evaluation
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Study
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Translational Medicine

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Deal

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Core Patent

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Clinical Trial

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Approval

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Biosimilar

Competitive landscape of biosimilars in different countries/locations. Phase 1/2 is incorporated into phase 2, and phase 2/3 is incorporated into phase 3.
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Competitive landscape of biosimilars in different countries/locations. Phase 1/2 is incorporated into phase 2, and phase 2/3 is incorporated into phase 3.

Regulation

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