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COMPANY

Kodiak Sciences

HQ: Palo Alto, CA source · kodiak.com ↗

Clinical Phase 3

10 open jobs · last seen Oct 23, 2026 · 12 sources

Ursus, Kodiak’s custom commercial scale manufacturing facility designed for complex antibody conjugate biotherapies, is successfully commissioned as a cGMP facility for Kodiak’s ABCD medicines. From company website Source · Oct 12, 2026

Keywords: antibody Wet Age-related Macular Degeneration Diabetic Macular Edema Macular Edema Secondary to Inflammation Retinal Vein Occlusion Diabetic Retinopathy Non-proliferative Diabetic Retinopathy Wet Macular Degeneration Macular Edema KSI-301 KSI-101 Tarcocimab

Location: Palo Alto, CA · source · Oct 14, 2026

Profile checked Oct 10, 2026

10Open jobs12Trials (company is sponsor)

Hiring

TitleLocation (from posting)Employer postedFirst seen
Senior IT / Security EngineerLocation not statedNot statedOct 16, 2026
Director, BiostatisticsLocation not statedNot statedOct 11, 2026
Senior Manager / Manager, Clinical Data ManagementLocation not statedNot statedOct 11, 2026
Polymer ChemistLocation not statedNot statedOct 11, 2026
Scientist, Organic ChemistryLocation not statedNot statedOct 11, 2026

See all 10 jobs

Trial and FDA signals

Job counts as of Oct 18, 2026. All trial and FDA signals

Timeline

  1. Trial start Phase 3: A Study to Evaluate the Efficacy and Safety of Tabirafusp Tedromer Compared to Aflibercept in Participants With DME - ALTO source ↗
  2. Trial start 3: A Phase 3 Study to Evaluate the Efficacy and Safety of Intravitreal KSI-101 in Participants With Macular Edema Secondary to Inflammation (MESI) - PEAK source ↗
  3. Trial start 3: A Phase 3 Study to Evaluate the Efficacy and Safety of Intravitreal KSI-101 in Participants With Macular Edema Secondary to Inflammation (MESI) - PINNACLE source ↗
  4. Trial start Phase 3: A Study to Evaluate the Efficacy and Safety of Tarcocimab Tedromer and Tabirafusp Tedromer Compared to Aflibercept in Participants With Neovascular (Wet) Age-related Macular Degeneration (wAM source ↗
  5. Trial start Phase 3: A Study to Evaluate the Efficacy and Safety of Tarcocimab Tedromer Compared With Sham Treatment in Participants With Diabetic Retinopathy (DR) source ↗
  6. Trial start Phase 3: A Study to Evaluate the Efficacy and Safety of Intravitreal KSI-301 in Non-proliferative Diabetic Retinopathy (NPDR) source ↗
  7. Trial start Phase 3: A Study to Evaluate the Efficacy and Safety of Intravitreal KSI-301 Compared With Intravitreal Aflibercept in Participants With Neovascular (Wet) Age-related Macular Degeneration (wAMD) source ↗
  8. Trial start Phase 3: A Trial to Evaluate the Efficacy, Durability, and Safety of KSI-301 Compared to Aflibercept in Participants With Diabetic Macular Edema (DME) source ↗
  9. Trial start Phase 3: A Study to Evaluate the Efficacy, Durability, and Safety of KSI-301 Compared to Aflibercept in Participants With Diabetic Macular Edema (DME) source ↗
  10. Trial start Phase 3: A Study to Evaluate the Efficacy, Durability, and Safety of KSI-301 Compared to Aflibercept in Patients With Macular Edema Due to Retinal Vein Occlusion (RVO) source ↗
  11. Trial start Phase 2/Phase 3: A Study to Evaluate the Efficacy and Safety of KSI-301, an Anti-VEGF Antibody Biopolymer Conjugate, Versus Aflibercept in Patients With Neovascular (Wet) Age-Related Macular Degenerat source ↗
  12. Trial start Phase 1: Exploratory Study to Investigate the Bioactivity, Ocular and Systemic Safety, Tolerability, and Pharmacokinetics Following Single and Multiple Intravitreal Administrations of KSI-301 in Subje source ↗

Upcoming milestones

Estimated primary completion per ClinicalTrials.gov. Dates move.

Clinical trials (lead sponsor) 12

RecordTitlePhaseStatusStartPrimary completion
NCT07734844A Study to Evaluate the Efficacy and Safety of Tabirafusp Tedromer Compared to Aflibercept in Participants With DME - ALTOPhase 3RecruitingAug 3, 2026Aug 31, 2028 (estimated)
NCT06996080A Phase 3 Study to Evaluate the Efficacy and Safety of Intravitreal KSI-101 in Participants With Macular Edema Secondary to Inflammation (MESI) - PINNACLE3RecruitingJul 16, 20252027-02 (estimated)
NCT06990399A Phase 3 Study to Evaluate the Efficacy and Safety of Intravitreal KSI-101 in Participants With Macular Edema Secondary to Inflammation (MESI) - PEAK3RecruitingJul 30, 20252027-04 (estimated)
NCT06270836A Study to Evaluate the Efficacy and Safety of Tarcocimab Tedromer Compared With Sham Treatment in Participants With Diabetic Retinopathy (DR)Phase 3CompletedMay 1, 2024Feb 13, 2026 (actual)
NCT06556368A Study to Evaluate the Efficacy and Safety of Tarcocimab Tedromer and Tabirafusp Tedromer Compared to Aflibercept in Participants With Neovascular (Wet) Age-related Macular Degeneration (wAMD) - DAYBREAKPhase 3Active, not recruitingAug 23, 20242026-08 (estimated)
NCT05066230A Study to Evaluate the Efficacy and Safety of Intravitreal KSI-301 in Non-proliferative Diabetic Retinopathy (NPDR)Phase 3TerminatedSep 7, 2021Aug 3, 2023 (actual)
NCT04611152A Trial to Evaluate the Efficacy, Durability, and Safety of KSI-301 Compared to Aflibercept in Participants With Diabetic Macular Edema (DME)Phase 3TerminatedSep 30, 2020May 11, 2023 (actual)
NCT04603937A Study to Evaluate the Efficacy, Durability, and Safety of KSI-301 Compared to Aflibercept in Participants With Diabetic Macular Edema (DME)Phase 3TerminatedSep 30, 2020Apr 27, 2023 (actual)
NCT04049266A Study to Evaluate the Efficacy and Safety of KSI-301, an Anti-VEGF Antibody Biopolymer Conjugate, Versus Aflibercept in Patients With Neovascular (Wet) Age-Related Macular Degeneration.Phase 2/Phase 3TerminatedOct 8, 2019Nov 17, 2021 (actual)
NCT04964089A Study to Evaluate the Efficacy and Safety of Intravitreal KSI-301 Compared With Intravitreal Aflibercept in Participants With Neovascular (Wet) Age-related Macular Degeneration (wAMD)Phase 3CompletedJun 23, 2021Mar 28, 2023 (actual)
NCT04592419A Study to Evaluate the Efficacy, Durability, and Safety of KSI-301 Compared to Aflibercept in Patients With Macular Edema Due to Retinal Vein Occlusion (RVO)Phase 3CompletedSep 25, 2020Jun 10, 2022 (actual)
NCT03790852Exploratory Study to Investigate the Bioactivity, Ocular and Systemic Safety, Tolerability, and Pharmacokinetics Following Single and Multiple Intravitreal Administrations of KSI-301 in Subjects With wAMD, DME and RVOPhase 1TerminatedDec 26, 2018Jun 2, 2021 (actual)

Open jobs 10

TitleLocation (from posting, not HQ)Employer postedFirst seenLevel
Senior IT / Security EngineerNot listedNot statedOct 16, 2026Not stated
Director, BiostatisticsNot listedNot statedOct 11, 2026Not stated
Senior Manager / Manager, Clinical Data ManagementNot listedNot statedOct 11, 2026Not stated
Polymer ChemistNot listedNot statedOct 11, 2026Not stated
Scientist, Organic ChemistryNot listedNot statedOct 11, 2026Not stated
Senior Electrical Engineer — VETi PlatformNot listedNot statedOct 11, 2026Not stated
Senior Optical Engineer — VETi PlatformNot listedNot statedOct 11, 2026Not stated
Senior Software Engineer — VETi PlatformNot listedNot statedOct 11, 2026Not stated
Associate Director, Quality OperationsNot listedNot statedOct 11, 2026Not stated
Research Associate, Quality OperationsNot listedNot statedOct 11, 2026Not stated

Level (Entry/Mid/Senior/Executive) is estimated from the job title and required years of experience. Descriptions are short excerpts (about the first 60 words) of the posting plus skills picked out of it; use Read full posting for the complete text.

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LinkedIn page linked from the company's own site: source · seen 2026-10-18

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