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Organization (Industry)

Kiora Pharmaceuticals, Inc.

ClinicalTrials.gov lists Kiora Pharmaceuticals, Inc. as lead sponsor of 18 trials. It has 7 active development programs and 1 approved asset.

US Industry Manufacturer CIK 0001372514

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3 0 2008 2026 2015 2020

Trials started per year with this organization as sponsor or collaborator, 1990 onward. The series also counts trials where the organization is a collaborator; the lead-sponsor trial count does not.

2026 is partial: 0 registered with a 2026 start date. The dashed outline is the pace from the 0 registered with a start date through October, planned starts included, not adjusted; not a forecast. No forecast is made for this organization: it averages 1.0 trial starts a year over the five years to October, under the 5 a year the method needs.

This page covers Kiora Pharmaceuticals, Inc.: 18 lead-sponsored trials and 3 legal-entity registrations.

Related companies are recorded in the same corporate group by GLEIF, ROR or a curator but are not grouped here; they are listed below with their own counts and are not included in the figures above.

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Disease areas (13)

Shown in this order: most trials first.

Disease areas
Disease area Trials
Dry Eye Syndromes 3
Uveitis 3
Uveitis, Anterior 3
Cataract 2
Macular Degeneration 2

Trials by start year as sponsor or collaborator (12)

Shown in this order: most recent first. 2026 is partial: trials registered with a 2026 start date so far, not a full year.

Show the table of trials by start year as sponsor or collaborator
Trials by start year as sponsor or collaborator
Year Trials started
2025 2
2023 1
2022 2
2019 1
2018 1
2017 1
2016 2
2015 2
2012 1
2011 1

Recruitment duration, a model prediction: 2 trials still running at the 2026-10-09 snapshot, fewer than the 5 needed for a median. Source: ClinicalTrials.gov / AACT (CTTI), public domain.

Active development programs (7)

Shown in this order: max phase, then active trials.

Active development programs
Drug Disease area Max phase Trials Ownership basis
KIO-104 Macular Degeneration Phase 2 1 Experimental arm
KIO-104 Macular Edema Phase 2 1 Experimental arm
50 μg KIO-301 Retinitis Pigmentosa Phase 2 1 Experimental arm
100 μg KIO-301 Retinitis Pigmentosa Phase 2 1 Experimental arm
KIO-101 Dry Eye Syndromes Phase 2 1 Backbone

Approved assets (1)

Approved assets
Drug Trials Ownership basis
DEXAMETHASONE 1 Generic, not holder

Sponsor delivery record (1)

Enrollment hit target: the share of this sponsor's lead-sponsored trials whose actual enrollment reached the planned enrollment. On time: the share whose actual primary completion date was no later than the planned date. Each share counts only trials where we observed an estimated figure before the actual one, and n is that number of trials. Below 5 trials the count is shown as a fraction, not a percentage.

Sponsor delivery record
Enrollment Timeline
67% hit target (n=6) 20% on time (n=5)

Journals published in (2)

Shown in this order: most published in first.

Journals published in
Journal Publications
Frontiers in medicine 1
Journal of cataract and refractive surgery 1

US granted patents (1)

Patents are not classified by disease area in the source, so this is the organization's overall portfolio, not a split by disease.

US granted patents
US patents granted Granted in the last 5 years Most recent grant
25 4 2025-07-22

SEC-reported annual financials (11)

Shown in this order: newest fiscal year first; SEC EDGAR XBRL companyfacts; non-USD filers converted to USD at the annual average rate.

SEC-reported annual financials
Fiscal year Revenue Net income R&D
2025 $0 -$10.8M $10.8M
2024 $16.0M $3.59M $7.84M
2023 $0 -$12.5M $4.03M
2022 not reported -$13.6M $3.45M
2021 $0 -$13.8M $5.35M
2020 $12.1K -$8.09M $3.57M
2019 $2.69M -$7.10M $5.39M
2018 $1.65M -$10.8M $8.06M
2017 $408K -$13.2M $10.3M
2016 $669K not reported $8.42M

Cash runway about 4.7 years at the end of FY2025. Estimate, derived not reported: $17.1M of cash and investments over $3.65M a year of net cash used in operations, averaged over the 3 reported fiscal years to FY2025. Latest-quarter runway about 20 months at 30 Jun 2026. Estimate, derived not reported: $16.8M of cash and investments at 30 Jun 2026 over $2.53M a quarter of net cash used in operations, averaged over the two quarters to 30 Jun 2026 (SEC 10-Q and 10-K filings).

Financing and grant events (41)

Shown in this order: most recent first; amounts in US dollars.

Financing and grant events
Date Round type Amount Source
2026-06-10 Other financing not disclosed SEC extracted
2026-05-28 Other financing not disclosed EDGAR offerings
2026-04-06 Private placement $5 SEC extracted
2026-04-06 Private placement $5.00M Form d
2025-09-15 Follow-on offering not disclosed EDGAR offerings

Climate targets, as filed (1)

Climate targets, as filed
Reporting year Net-zero target
2025 not disclosed

Workforce and board diversity, as filed (1)

Workforce and board diversity, as filed
Reporting year Workforce % women Board % women
2025 not disclosed not disclosed

Latest dated events (84)

Shown in this order: newest first.

Latest dated events
Date Event Source
2026-06-10 Financing Funding rounds and grants (NIH RePORTER + SEC EDGAR)
2026-05-28 Financing Funding rounds and grants (NIH RePORTER + SEC EDGAR)
2026-04-06 Private placement Funding rounds and grants (NIH RePORTER + SEC EDGAR)
2026-04-06 Private placement Funding rounds and grants (NIH RePORTER + SEC EDGAR)
2025-09-15 Follow-on offering Funding rounds and grants (NIH RePORTER + SEC EDGAR)

Biomarker capability evidence (10)

Shown in this order: tier desc, then gene symbol.

Biomarker capability evidence
Gene Role Evidence
CHM Trial sponsor Named in trial inclusion criteria
NINL Trial sponsor Named in trial inclusion criteria
NINL Trial sponsor Named in trial inclusion criteria
AATF Trial sponsor Named in trial exclusion criteria
TNF Trial sponsor Named in trial exclusion criteria

Not on this page

Checked, with nothing recorded for this organization: companies grouped under this page, fda warning letters, fda untitled letters, fda inspection record, fda recalls, fda import refusals, manufacturing and distribution sites, organization relationships, clia clinical laboratory certificates, and biomarkers this organization publishes on.