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PF-06473871

Alternative Names: pf-06473871, pf06473871, pf 06473871
Clinical Status: Inactive
Latest Update: 2021-08-13
Latest Update Note: Clinical Trial Update

Product Description

The antisense oligonucleotide, PF-06473871, comprises a 20-nucleotide chain containing a phosphorothioate backbone and 2Õ-methoxyethyl modifications of the ribose units at the 3Õ and 5Õ ends, conferring resistance to nucleases and providing long residence in tissues. PF-06473871 targets CTGF expression and is delivered by intradermal injection to a surgical wound. (Sourced from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6191237/)

Mechanisms of Action: CTGF Inhibitor

Novel Mechanism: Yes

Modality: Nucleic Acid

Route of Administration: Injection

FDA Designation: *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Pfizer
Company Location: Eastern America
Company CEO: Albert Bourla
Additional Commercial Interests: None

Clinical Description

Countries in Clinic:

Active Clinical Trial Count:

Recent & Upcoming Milestones

Highest Development Phases

Phase 2: Healthy Volunteers|Vision, Low|Other

Phase 1: Healthy Volunteers

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

NCT01753791

B5301002

P1

Completed

Healthy Volunteers

2013-06-01

2019-03-19

Treatments

NCT02205476

B5301012

P2

Terminated

Vision, Low

2015-01-01

2019-03-20

Treatments

2012-004355-37

2012-004355-37

P2

Completed

Unknown

2014-10-17

2022-03-13

Treatments

NCT01730339

B5301001

P2

Completed

Healthy Volunteers

2014-10-01

2019-03-19

NCT01494922

EXC 001-206

P2

Completed

Other

2013-09-10

2021-08-14

Primary Completion Date|Primary Endpoints|Start Date|Study Completion Date|Treatments

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