Last update 08 May 2025

LY-3084077

Overview

Basic Info

Drug Type
Synthetic peptide
Synonyms
Target-
Action-
Mechanism-
Therapeutic Areas-
Active Indication-
Inactive Indication-
Originator Organization
Eli Lilly & Co.Eli Lilly & Co.
Active Organization-
Inactive Organization
Eli Lilly & Co.Eli Lilly & Co.
License Organization-
Drug Highest PhasePendingPhase 1
First Approval Date-
Regulation-
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Related

1
Clinical Trials associated with LY-3084077
NCT01846702
/ CompletedPhase 1
A Single-Dose, Dose-Escalation Study to Determine the Safety, Tolerability, and Pharmacokinetics of LY3084077 in Healthy Subjects
100 Clinical Results associated with LY-3084077
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100 Translational Medicine associated with LY-3084077
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100 Patents (Medical) associated with LY-3084077
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100 Deals associated with LY-3084077
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R&D Status

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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date
NCT01846702 (CTgov)
Phase 1
-
43
Placebo
(Placebo Cohort 1)
keheshfvxh(beeztkowqb) = xbrdhhevtw zidugkaeet (nneauayqcn, wezzrcchqq - qzccqxnndd)
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-
30 Jul 2018
(LY3084077 Cohort 2)
keheshfvxh(beeztkowqb) = yepxjubeno zidugkaeet (nneauayqcn, nadnuazixb - anjvadkthp)
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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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