Last update 20 Mar 2025

Teriparatide Acetate( Asahi Kasei Pharma)

Overview

Basic Info

Drug Type
Synthetic peptide
Synonyms
Teriparatide Acetate, Teribone
+ [1]
Target
PTH1R
Action
agonists
Mechanism
PTH1R agonists(Parathyroid hormone receptor agonists)
Therapeutic Areas
Endocrinology and Metabolic DiseaseSkin and Musculoskeletal Diseases
Active Indication
Osteoporosis
Inactive Indication-
Originator Organization
Asahi Kasei Pharma Corp.Asahi Kasei Pharma Corp.
Active Organization
Asahi Kasei Pharma Corp.Asahi Kasei Pharma Corp.
Inactive Organization-
Drug Highest PhaseApproved
First Approval Date
Japan (26 Sep 2011),
Osteoporosis
Regulation-
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Structure/Sequence

Related

4
Clinical Trials associated with Teriparatide Acetate( Asahi Kasei Pharma)
JPRN-JapicCTI-205137
/ CompletedNot ApplicableIIT
Searching study for comparative examination in Forteo and Teribone in an osteoporosis patient after menopause
JPRN-UMIN000037146
/ SuspendedNot ApplicableIIT
A randomized comparative study between the parallel group to evaluate the efficacy of drinking some water immediately before the administration of Teriparatide acetate for preventing the incidence of nausea - A comparative study of efficacy of drinking water on declining the incidence of nausea after administration of Teriparatide acetate
KCT0004153
/ RecruitingPhase 1IIT
A randomized, open-label, single dose, 2-sequence, 2-period crossover study to explore the safety and pharmacokinetic characteristics of Teribone injection 56.5ug and Rap18001 in postmenopausal female volunteers
100 Clinical Results associated with Teriparatide Acetate( Asahi Kasei Pharma)
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100 Translational Medicine associated with Teriparatide Acetate( Asahi Kasei Pharma)
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100 Patents (Medical) associated with Teriparatide Acetate( Asahi Kasei Pharma)
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100 Deals associated with Teriparatide Acetate( Asahi Kasei Pharma)
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R&D Status

10 top approved records.
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IndicationCountry/LocationOrganizationDate
Osteoporosis
Japan
Asahi Kasei Pharma Corp.Asahi Kasei Pharma Corp.
26 Sep 2011
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date

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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

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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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