Effect of Intravitreally Administered AIV007 in Subjects With Neovascular Age-Related Macular Degeneration (nAMD)

AiViva BioPharma

Status and phase: Completed; Phase 1

Conditions: Neovascular Age-related Macular Degeneration

Treatments: Drug: AIV007

Study type: Interventional

Funder types: Industry

Identifiers

NCT04422899

AIV007-E01

Details and patient eligibility

About

To determine safety, pharmacokinetics, and duration of effect of intravitreally administered AIV007 gel suspension in subjects with neovascular age-related macular degeneration

Full description

AIV007 is a multiple kinase inhibitor of vascular endothelial growth factor receptors (VEGFR 1, -2 & -3); fibroblast growth factor receptors (FGFR-1, -2, -3 & -4); and platelet-derived growth factor receptors (PDGFR-α & β)1. Lenvatinib is the active pharmaceutical ingredient in AIV007 formulation that is FDA-approved for oral administration for patients with advanced renal cell carcinoma (RCC), differentiated thyroid cancer (DTC), unresectable hepatocellular carcinoma (HCC), and advanced endometrial carcinoma (Lenvima USPI 2021; NDA 206947). AIV007 is a novel, thermoresponsive gel suspension for intravitreal administration proposed to form a durable depot inside the eye. This monotherapy is being evaluated for the treatment of retinal and choroidal vascular disease. A single intravitreal treatment in 3 subjects was evaluated using 2 doses to evaluate depot formation, safety and biological activity by measuring visual acuity, reduction in retinal fluids associated with vision and effects of fibrosis.

Enrollment: 3 patients

Sex: All

Ages: 50+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Male or female subjects aged ≥ 50 years

2. Subjects must provide written informed consent before any study-related procedures are performed

3. Active subfoveal CNV in the study eye secondary to AMD that has previously been treated with at least 3 intravitreal injections of an anti-VEGF agent

4. BCVA in the study eye

   1. Sentinel subjects only: 65 ETDRS letters (20/50 Snellen equivalent) or worse
   2. All other subjects: 78 to 35 ETDRS letters (20/32 to 20/200 Snellen equivalent)

5. Clear ocular media and adequate pupil dilation in both eyes to permit good quality photographic imaging

Exclusion criteria

1. Previous treatment for nAMD in the study eye, other than standard-of-care anti- VEGF IVT injection, eg, cell therapy, brachytherapy, gene therapy
2. Treatment with anti-VEGF in the non-study eye 2 weeks prior to baseline
3. Presence of diabetic retinopathy or glaucoma in either eye
4. Spherical equivalent for refractive error in the study eye of worse than 8.0 diopters of myopia (prior to cataract or refractive surgery)
5. Presence of active infection or inflammation within 30 days prior to screening
6. Presence of contraindications to anti-VEGF treatment, including myocardial infarction, any cardiac event requiring hospitalization, treatment for acute congestive heart failure, transient ischemic attack, or stroke within the last 3 months of baseline
7. Uncontrolled hypertension or diabetes mellitus

Trial design

Primary purpose: Treatment

Allocation: Non-Randomized

Interventional model: Sequential Assignment

Masking: None (Open label)

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3 participants in 3 patient groups

AIV007 Treatment Dose 1

Experimental group

Description:

Intravitreal, Dose 1

Treatment:

Drug: AIV007

AIV007 Treatment Dose 2

Experimental group

Description:

Intravitreal, Dose 2

Treatment:

Drug: AIV007

AIV007 Treatment Dose 3

Experimental group

Description:

Intravitreal, Dose 3

Treatment:

Drug: AIV007