Nicotinamide for Retinal Protection in Primary Open-Angle Glaucoma (NADIR Trial) (NADIR)

NADIR Trial: A Principal Investigator-Initiated, Single-Center, Open-Label, Active-Controlled Phase 2a Study of High-Dose Nicotinamide (Vitamin B3) Supplementation in Adults With Mild to Moderate Primary Open-Angle Glaucoma (POAG)

The goal of this clinical trial is to learn whether a high-dose vitamin B3 supplement called nicotinamide can protect retinal nerve cells in adults with primary open-angle glaucoma (POAG) who are already receiving standard glaucoma eye drops or laser treatment. The main question it aims to answer is: Does adding nicotinamide to standard glaucoma therapy slow the rate of thinning of the inner retinal nerve cell layer (measured by a non-invasive eye scan) compared to standard therapy alone over 12 months?

Participants will be randomly assigned to one of two groups. Participants in the treatment group will take nicotinamide tablets by mouth, starting at a lower dose (1.5 grams per day) for the first 6 weeks and increasing to the full dose (3.0 grams per day) for the remainder of the 12-month study. Participants in the control group will continue their standard glaucoma care without the supplement.

Researchers will compare retinal imaging measurements between the two groups to see whether nicotinamide reduces the rate of retinal nerve cell thinning over time.

Study Overview

• Status: Not yet recruiting
• Conditions: Primary Open Angle Glaucoma (POAG); Glaucoma, Open-angle
• Intervention / Treatment: Drug: Nicotinamide; Other: Standard Glaucoma Therapy

Detailed Description

Glaucoma causes progressive and irreversible loss of retinal ganglion cells (RGCs), often continuing despite adequate intraocular pressure control. Mitochondrial dysfunction and depletion of NAD+ (nicotinamide adenine dinucleotide) are increasingly recognized as central contributors to RGC vulnerability. Nicotinamide (NAM), a commercially available form of vitamin B3 and potent NAD+ precursor, has demonstrated robust neuroprotection in preclinical glaucoma models and early clinical trials outside the United States.

NADIR is the first IND-regulated, prospective, randomized Phase 2a trial in the United States to evaluate high-dose oral nicotinamide as adjunctive neuroprotective therapy in adults with mild to moderate POAG, using macular ganglion cell layer imaging (SD-OCT) as the primary structural biomarker detectable within 12 months. Ocular vascular perfusion imaging (OCT-A) is included as an exploratory endpoint.

• Study Type: Interventional
• Enrollment (Estimated): 96
• Phase: Phase 2

Contacts and Locations

• Study Contact: Name: Steven C Quan, OD; Phone Number: 773-702-1611; Email: scquan@bsd.uchicago.edu
• Study Contact Backup: Name: Elza Rachid, MD; Phone Number: 773-702-1611; Email: Elza.Rachid@bsd.uchicago.edu

Study Locations

• United States
  • Illinois
    • Chicago, Illinois, United States, 60637
      • University of Chicago Medicine Duchossois Center for Advanced Medicine
      • Contact: Steven C Quan, OD; Phone Number: 773-702-1611; Email: scquan@bsd.uchicago.edu
      • Contact: Elza Rachid, MD; Phone Number: 773-702-1611; Email: Elza.Rachid@bsd.uchicago.edu

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Adult; Older Adult
• Accepts Healthy Volunteers: No

Description

Inclusion Criteria:

• Age 40 to 80 years, inclusive
• Diagnosis of primary open-angle glaucoma (POAG) in at least one eye, confirmed by a licensed ophthalmologist or optometrist based on characteristic optic nerve head changes and/or visual field defects with an open anterior chamber angle
• Mild to moderate glaucoma severity in the study eye: Humphrey Visual Field 24-2 mean deviation (MD) between -2.0 and -12.0 dB on at least one reliable test (fixation losses 33% or less, false positive rate 15% or less)
• Best-corrected visual acuity (BCVA) of 20/40 or better (Snellen equivalent) in the study eye
• Confirmed glaucomatous structural damage on SD-OCT (average GCIPL and/or RNFL below age-adjusted normative mean on device-generated classification) and/or a reproducible visual field defect on Humphrey Visual Field 24-2 consistent with glaucoma, as confirmed by the enrolling glaucoma specialist at screening
• Macular GCIPL and peripapillary RNFL above device-specific SD-OCT floor effect in the study eye
• Currently receiving stable intraocular pressure-lowering therapy (topical medications and/or prior selective laser trabeculoplasty) for at least 4 months prior to enrollment, with no planned changes to glaucoma therapy at the time of enrollment
• Intraocular pressure of 21 mmHg or less on current therapy at the screening visit in the study eye
• Established patient receiving ongoing glaucoma care at University of Chicago Medicine Duchossois Center for Advanced Medicine Eye Clinic
• Willing and able to provide written informed consent and comply with all study visit schedules and procedures

Exclusion Criteria:

• Advanced glaucoma: visual field MD worse than -12.0 dB or BCVA worse than 20/40 in the study eye
• Significant retinal disease affecting macular structure or visual field, including advanced age-related macular degeneration, diabetic retinopathy greater than mild non-proliferative, clinically significant diabetic macular edema, major retinal vein occlusion, or non-glaucomatous optic neuropathy
• Ocular surgery other than uncomplicated cataract extraction or selective laser trabeculoplasty within the past 6 months
• Hepatic dysfunction at baseline: AST or ALT greater than 2 times the upper limit of normal, or total bilirubin greater than 1.5 times the upper limit of normal
• Renal dysfunction: eGFR less than 30 mL/min/1.73 m2
• Current use of, or unwillingness to abstain from: NAD+/nicotinamide supplements, high-dose niacin or vitamin B3, Ginkgo biloba, CoQ10, isoniazid, pyrazinamide, carbamazepine, phenobarbital, primidone, or sustained-release niacin or nicotinamide formulations
• Poorly controlled diabetes mellitus: HbA1c greater than 9.0% at screening
• Normal tension glaucoma with documented intraocular pressure consistently 21 mmHg or less without hypotensive therapy
• Participation in another investigational drug trial within 30 days of screening
• Pregnancy, lactation, or intent to become pregnant during the study period
• Significant cognitive impairment or inability to comply with study requirements
• Clinically significant media opacity (corneal, lenticular, or vitreal) sufficient to degrade OCT signal quality below device-minimum thresholds, even if BCVA of 20/40 or better is preserved
• Active or recent uveitis or intraocular inflammation in the study eye within the past 3 months
• Any condition that, in the investigator's judgment, would preclude safe participation or confound result interpretation

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: None (Open Label)

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: High-Dose Oral Nicotinamide Plus Standard Glaucoma Care; Participants receive immediate-release oral nicotinamide titrated from 1.5 g/day (500 mg three times daily with meals, Weeks 1 through 6) to 3.0 g/day (1,500 mg twice daily [three 500 mg tablets per administration, twice daily] with meals, Week 7 through Month 12), in addition to individualized standard glaucoma therapy. Dose advancement at Week 7 requires confirmation at the Month 1 remote safety contact that no Grade 2 or higher hepatic adverse event is present and gastrointestinal tolerability is acceptable.	Drug: Nicotinamide; Immediate-release nicotinamide 500 mg tablets (NDC 0-80681-01900; Rugby Laboratories / Contract Pharmacal Corp, Hauppauge NY). Titration phase: 500 mg three times daily (1.5 g/day total) for 6 weeks. Maintenance phase: 1,500 mg twice daily (three 500 mg tablets per administration, twice daily; 3.0 g/day total) from Week 7 through Month 12. Administered orally with meals. Dispensed and tracked by the University of Chicago Institutional Drug Service (IDS) Pharmacy under IND 184022.; Other Names: Vitamin B3; Niacinamide; NAM; Rugby Niacinamide 500 mg; Other: Standard Glaucoma Therapy; Individualized intraocular pressure-lowering therapy per the 2026 American Academy of Ophthalmology Primary Open-Angle Glaucoma Preferred Practice Pattern. Includes topical prostaglandin analog eye drops and/or selective laser trabeculoplasty, with clinical monitoring by optical coherence tomography, standard automated perimetry, and intraocular pressure measurement at 3 to 6 month intervals based on disease status.
Active Comparator: Standard Glaucoma Care Alone (Active Control); Participants receive individualized standard glaucoma therapy per the 2026 American Academy of Ophthalmology Primary Open-Angle Glaucoma Preferred Practice Pattern, including intraocular pressure lowering with topical prostaglandin analogs and/or selective laser trabeculoplasty, with monitoring by optical coherence tomography, perimetry, and intraocular pressure measurement at 3 to 6 month intervals. No supplemental nicotinamide is administered.	Other: Standard Glaucoma Therapy; Individualized intraocular pressure-lowering therapy per the 2026 American Academy of Ophthalmology Primary Open-Angle Glaucoma Preferred Practice Pattern. Includes topical prostaglandin analog eye drops and/or selective laser trabeculoplasty, with clinical monitoring by optical coherence tomography, standard automated perimetry, and intraocular pressure measurement at 3 to 6 month intervals based on disease status.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Annualized Rate of Macular Ganglion Cell-Inner Plexiform Layer (GCIPL) Thinning	Rate of change in macular GCIPL thickness (micrometers per year) measured by spectral-domain optical coherence tomography (SD-OCT; Heidelberg Spectralis, minimum Q-score 20) with masked central image reading using de-identified participant IDs. The annualized thinning rate is estimated from repeated measurements using a linear mixed-effects model with random intercepts per participant and an arm-by-time interaction term as the primary inferential parameter.	Baseline (Month 0), Month 3, Month 6, and Month 12 (four repeated assessments over 12 months)

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Annualized Rate of Peripapillary Retinal Nerve Fiber Layer (RNFL) Thinning	Rate of change in average peripapillary RNFL thickness (micrometers per year) measured by SD-OCT (Heidelberg Spectralis) with masked central reading. Analyzed using the same linear mixed-effects model framework as the primary endpoint. Both average and quadrant-specific RNFL (superior, inferior, temporal, nasal) will be reported.	Baseline (Month 0), Month 3, Month 6, and Month 12 (four repeated assessments over 12 months)
Visual Field Mean Deviation Slope	Rate of change in Humphrey Visual Field Analyzer 24-2 SITA Standard mean deviation (decibels per year), estimated as a continuous slope over 12 months using a linear mixed-effects model with random intercepts per participant. Assessed at four timepoints: Baseline, Month 3, Month 6, and Month 12.	Baseline through Month 12, assessed at Baseline (Month 0), Month 3, Month 6, and Month 12
Incidence of Grade 2 or Higher Hepatic and Gastrointestinal Adverse Events	Proportion of participants experiencing at least one hepatic adverse event (alanine aminotransferase or aspartate aminotransferase elevation, total bilirubin elevation) or gastrointestinal adverse event graded at Grade 2 or higher per the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE v6.0). Hepatic laboratory values assessed by comprehensive metabolic panel (CMP) at every study visit and at the Month 1 remote safety contact for all participants in both arms.	From randomization through 30 days after the Month 12 visit (approximately 13 months)
Nicotinamide Adherence Rate	Proportion of prescribed nicotinamide doses taken during the maintenance phase (Weeks 7 through 52), assessed by pill count and participant medication diary review at each in-person study visit. Applies to Arm 1 participants only.	Maintenance phase: Week 7 (Month 1 remote contact) through Month 12
Study Retention Rate	Proportion of randomized participants completing the Month 12 study visit with at least one valid post-baseline macular GCIPL measurement. Assessed in both arms.	Month 12 (52 weeks post-randomization)

Other Outcome Measures

Outcome Measure	Measure Description	Time Frame
Change in Macular Superficial Capillary Plexus Perfusion Density on OCT-A	Change from baseline in macular superficial capillary plexus perfusion density (percent) measured by optical coherence tomography angiography (OCT-A; Optovue Solix FullRange AngioVue, FDA 510(k) K222166; minimum signal strength index 30). Analyzed by ANCOVA with baseline perfusion density as covariate. Designated an exploratory endpoint in this Phase 2a trial; not a pre-specified confirmatory secondary outcome.	Baseline (Month 0) and Month 12 (pre- and post-intervention comparison)
Change in Peripapillary Radial Capillary Plexus Perfusion Density on OCT-A	Change from baseline in peripapillary radial capillary plexus (RPC) perfusion density (percent) measured by optical coherence tomography angiography (OCT-A; Optovue Solix FullRange AngioVue, FDA 510(k) K222166; minimum signal strength index 30). Analyzed by ANCOVA with baseline peripapillary perfusion density as covariate and treatment arm as fixed factor. Macular and peripapillary perfusion density metrics are analyzed and reported separately. Designated an exploratory endpoint in this Phase 2a trial.	Baseline (Month 0) and Month 12 (pre- and post-intervention comparison)

Collaborators and Investigators

• Sponsor: University of Chicago
• Investigators: Principal Investigator: Steven C Quan, OD, University of Chicago

Study record dates

Study Major Dates

• Study Start (Estimated): June 1, 2027
• Primary Completion (Estimated): September 30, 2029
• Study Completion (Estimated): October 31, 2029

Study Registration Dates

• First Submitted: September 2, 2026
• First Submitted That Met QC Criteria: September 2, 2026
• First Posted (Actual): September 8, 2026

Study Record Updates

• Last Update Posted (Actual): September 8, 2026
• Last Update Submitted That Met QC Criteria: September 2, 2026
• Last Verified: September 1, 2026

More Information

Terms related to this study

• Keywords: NAD+; optical coherence tomography; neuroprotection; OCT-A; vitamin B3; nicotinamide; glaucoma progression; retinal ganglion cells; GCIPL; macular imaging
• Additional Relevant MeSH Terms: Eye Diseases; Ocular Hypertension; Glaucoma; Glaucoma, Open-Angle; Pyridines; Heterocyclic Compounds, 1-Ring; Heterocyclic Compounds; Acids, Heterocyclic; Nicotinic Acids; Niacinamide
• Other Study ID Numbers: IRB26-0972; IND Number: 184022 (Other Identifier: U.S. Food and Drug Administration (FDA))

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: YES
• IPD Plan Description: De-identified individual participant data supporting primary and secondary outcome analyses will be made available following study completion and primary manuscript publication, subject to University of Chicago data governance policies and a data use agreement. Requests will be reviewed by the principal investigator.
• IPD Sharing Time Frame: Beginning 12 months after primary study results publication
• IPD Sharing Access Criteria: Requests submitted to the principal investigator with a brief description of the proposed analysis and intended use. De-identified data shared under a formal data use agreement per University of Chicago institutional policy.
• IPD Sharing Supporting Information Type: STUDY_PROTOCOL; SAP; ICF

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: Yes
• Studies a U.S. FDA-regulated device product: No