Last update 23 Aug 2025

C2L-OCT-01 PR

Overview

Basic Info

Drug Type
Synthetic peptide
Synonyms-
Target-
Action-
Mechanism-
Therapeutic Areas
Nervous System DiseasesEndocrinology and Metabolic DiseaseSkin and Musculoskeletal Diseases+ [1]
Active Indication-
Inactive Indication
Acromegaly
Originator Organization
Ambrilia Biopharma, Inc.
Active Organization-
Inactive Organization
Ambrilia Biopharma, Inc.
License Organization-
Drug Highest PhaseDiscontinuedPhase 3
First Approval Date-
Regulation-
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Related

4
Clinical Trials associated with C2L-OCT-01 PR
NCT00642421
/ TerminatedPhase 3
Safety and Biological Activity of a New Prolonged Release Formulation of Octreotide Acetate, C2l-OCT-01 PR, Administered Intra Muscularly Every 4, 5 or 6 Weeks in Acromegalic Patients
EUCTR2007-004162-41-HU
/ Not yet recruitingNot Applicable
SAFETY AND BIOLOGICAL ACTIVITY OF A NEW PROLONGED RELEASE FORMULATION OF OCTREOTIDE ACETATE, C2L-OCT-01 PR, ADMINISTERED INTRA MUSCULARLY EVERY 6 WEEKS IN ACROMEGALIC PATIENTS
NCT00635765
/ CompletedPhase 3
Open Label Extension Study Evaluating the Safety and Biological Activity of a New Prolonged Release Formulation of Octreotide Acetate, C2L-OCT-01 PR, Administered Intra Muscularly Every 6, 5 or 4 Weeks in Acromegalic Patients
100 Clinical Results associated with C2L-OCT-01 PR
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100 Translational Medicine associated with C2L-OCT-01 PR
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100 Patents (Medical) associated with C2L-OCT-01 PR
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100 Deals associated with C2L-OCT-01 PR
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R&D Status

10 top R&D records.
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IndicationHighest PhaseCountry/LocationOrganizationDate
AcromegalyPhase 3
Belarus
Ambrilia Biopharma, Inc.
01 Apr 2007
AcromegalyPhase 3
Hungary
Ambrilia Biopharma, Inc.
01 Apr 2007
AcromegalyPhase 3
Romania
Ambrilia Biopharma, Inc.
01 Apr 2007
AcromegalyPhase 3
Serbia
Ambrilia Biopharma, Inc.
01 Apr 2007
AcromegalyPhase 3
Slovakia
Ambrilia Biopharma, Inc.
01 Apr 2007
AcromegalyPhase 3
Ukraine
Ambrilia Biopharma, Inc.
01 Apr 2007
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Clinical Result

Indication
Phase
Evaluation
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Phase
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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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