TegoScience is a leading company in the Korean cell therapeutics market.
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- 2001
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- 03 20Established in Daejeon, Korea
- 03Designated as 'High-tech Venture Company'
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- 2002
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- 03Moved to facility & head office in Seoul
- 09'Cutigen Research Institute' established
- 09Designated as 'Innovative Technology Company'
- 12 10Holoderm® approved /
Production & sales approval by KFDA
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- 2003
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- 04Qualified as GMP facility by KFDA
- 06Kaloderm®, IND approved
- 12Awarded excellence award at Korea Healthcare Technology Fair
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- 2004
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- 05First export shipment of Neoderm® to Japan
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- 2005
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- 03 21Kaloderm® approved for burns by KFDA
- 09Selected as technological innovation task
- 10Awarded silver medal at Korea Technology Fair
- 11Certified as KT(Korea Technology)
- 12Awarded prime minister’s medal at Korea Healthcare Technology Fair
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- 2006
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- 01Certified as HT(Health Technology)
- 041stSpecial Symposium
- 09Cultured keratinocyte registered as cosmetics ingredient
(CTFA, US)
- 12Designated as one of 10 best-new technologies
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- 2007
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- 03Worker’s Compensation reimbursement for both
Holoderm® and Kaloderm®
- 04Kaloderm® approved National Health Insurance reimbursement for burns
- 12Holoderm® Phase III clinical study completed after approval
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- 2008
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- 2010
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- 06Kaloderm® approved additionally for Diabetic Foot Ulcer
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- 2012
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- 02Technology transfer from Yonsei University: 'In vivo Induction
Methods for Migrating Stem Cells to a Target Site'
- 05Begined Neoderm® business for sales, distribution of cells
for research and contract research service
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- 2014
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- 11 06IPO: KOSDAQ [191420]
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- 2015
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- 05 06kaloderm® PMS (for diabetic foot ulcer) approved
- 09Designated as ‘K-Brain Power Company'
- 09TPX-105 [Autologous Cultured Fibroblasts] Phase II,
IND approved
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- 2016
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- 03Incorporated 'Cutigen Laboratories', biotechnology-based
cosmetics company as a subsidiary of Tego Science.
- 11Certified as 'Innovative Pharmaceutical Company'
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- 2017
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- 04Entered the cosmeceutical cosmetics business through
subsidiary, Cutigen Laboratories
- 11Completed new GMP facility and relocated head office
- 12Rosmir® approved by KFDA
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- 2018
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- 03TPX-114 Phase III, IND approved
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- 2019
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- 07Recertified as 'Innovative Pharmaceutical Company'
- 09Kaloderm® approved National Health Insurance reimbursement for Diabetic Foot Ulcer
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- 2020
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- 03TPX-115 Phase II, IND approved
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- 2021
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- 01Contracted Kaloderm® sales & marketing with SK Chemicals
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- 2022
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- 06Completed TPX-115 Phase I/II clinical trial
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- 2023
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- 03Selected for SME & Startup Structural Innovation Support R&D Program
- 05TPX-115 Phase IIb/III, IND approved
- 08Published paper demonstrating superiority of TPX-115 in international journal(AJSM)
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- 2024
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- 07Allogeneic nasolabial fold treatment(TPX-121) Phase I, IND approved
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- 2025
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- 02TPX-115 Phase II, IND approved by U.S. FDA
- 02Received Medical Device GMP Certification from MFDS
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- 2026
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- 01Completed TPX-121 Phase I clinical trial