Ozmosi | Abicipar pegol Drug Profile
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Abicipar pegol

Alternative Names: abicipar pegol, agn-150998, mp0112
Clinical Status: Inactive
Latest Update: 2023-07-01
Latest Update Note: PubMed Publication

Product Description

Abicipar Pegol is an anti-VEGF molecule based on the designed ankyrin repeat proteins (DARPin) therapeutics (Sourced from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7182559/)

Mechanisms of Action: VEGF Inhibitor

Novel Mechanism: No

Modality: Peptide/Protein

Route of Administration: Injection

FDA Designation: *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Company: AbbVie
Company Location: Eastern America
Company Founding Year: 2013
Additional Commercial Interests: None

Clinical Description

Countries in Clinic:

Active Clinical Trial Count:

Recent & Upcoming Milestones

Highest Development Phases

Phase 3: Macular Degeneration|Neovascular age-related macular degeneration

Phase 2: Macular Degeneration|Macular Edema

Phase 1: Macular Degeneration|Macular Edema|Wet Macular Degeneration

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

NCT03335852

PINE

P1

Completed

Macular Degeneration

2018-10-08

21%

2019-03-21

NCT02859766

NCT02859766

P1

Completed

Macular Degeneration

2017-10-20

2019-03-20

Treatments

NCT01042678

MP0112-CP02

P1

Terminated

Macular Edema

2010-12-01

2019-03-19

Treatments

NCT01086761

MP0112-CP01

P1

Terminated

Wet Macular Degeneration

2010-11-01

2019-03-19

Treatments

NCT03539549

NCT03539549

P2

Completed

Macular Degeneration

2019-02-27

59%

2020-08-05

NCT02181504

BAMBOO

P2

Completed

Macular Degeneration

2015-12-01

2019-03-20

Treatments

NCT02186119

PALM

P2

Completed

Macular Edema

2015-06-01

2019-03-20

Treatments

NCT02181517

CYPRESS

P2

Completed

Macular Degeneration

2015-03-01

2019-03-20

Treatments

2011-002526-43

REACH Study

P2

Completed

Macular Degeneration

2014-04-09

2022-03-13

Treatments

NCT01397409

REACH Study

P2

Completed

Macular Degeneration

2014-03-31

2019-04-17

Primary Completion Date|Study Completion Date|Treatments

2014-004579-22

CEDAR

P3

Completed

Neovascular age-related macular degeneration

2019-04-16

40%

2025-06-27

Treatments

2014-004580-20

SEQUOIA

P3

Completed

Neovascular age-related macular degeneration

2019-04-03

40%

2022-03-13

Treatments

NCT02462928

CEDAR

P3

Completed

Macular Degeneration

2018-04-18

40%

2020-07-29

Primary Endpoints|Treatments

NCT02462486

SEQUOIA Study

P3

Completed

Macular Degeneration

2018-04-12

40%

2020-07-31

Patient Enrollment|Primary Endpoints|Treatments