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KSI-601

Alternative Names: ksi-601, ksi 601, ksi601
Latest Update: 2022-07-21
Latest Update Note: Clinical Trial Update

Product Description

KSI-601 is a triplet biopolymer conjugate for the treatment of dry age-related macular degeneration. (Sourced from: https://kodiak.com/our-pipeline/)

Mechanisms of Action: Unknown

Novel Mechanism: No

Modality: N/A

Route of Administration: N/A

FDA Designation: None *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Kodiak Sciences
Company Location: PALO ALTO CA 94304
Company CEO: Victor Perlroth
Additional Commercial Interests: None

Clinical Description

Countries in Clinic:

Active Clinical Trial Count:

Highest Development Phases

Phase 0: Macular Degeneration

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Trial Status

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Primary Completion Date

Probability of Success

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