Aerpio Pharmaceuticals Presents Data from Fifth Patient Cohort Showing Potential of Topical Ocular Formulation of AKB-9778 Pr...
08 February 2020 - 10:20AM
Business Wire
Data presented at the 9th Annual Glaucoma 360
New Horizons Forum
Aerpio Pharmaceuticals, Inc. (Nasdaq: ARPO), a biopharmaceutical
company focused on developing compounds that activate Tie2 to treat
ocular diseases and diabetic complications, announced that Kevin
Peters, M.D., Aerpio’s Chief Scientific Officer, presented data
from the fifth cohort of subjects from a Phase 1b trial showing the
potential of a topical ocular formulation of AKB-9778, a VE-PTP
inhibitor and Tie2 activator, to lower intraocular pressure (IOP)
with minimal conjunctival hyperemia when combined with
standard-of-care prostaglandin therapy. The data were presented at
the Glaucoma 360 New Horizons Forum 2020, on February 7, in San
Francisco.
The presentation included an updated dataset from a Phase 1b
trial of a topical ocular formulation of AKB-9778 from the fifth
cohort of patients with ocular hypertension (OHT) or primary open
angle glaucoma (POAG). The updated results from the fifth cohort
will be posted on the Company’s website.
“We continue to be encouraged by the findings from Aerpio’s
topical ocular formulation of AKB-9778 in patients with ocular
hypertension or primary open angle glaucoma,” said Brian Levy D.O.,
M.Sc., CEO of at Ocunexus Therapeutics and former CMO of Aerie
Pharmaceuticals. “The IOP lowering observed when AKB-9778 was
combined with a prostaglandin in the fifth cohort of Aerpio’s Phase
1b trial was comparable to or better than those produced by common
commercial adjunctive therapies. Importantly, AKB-9778 achieved
this IOP lowering while causing minimal conjunctival hyperemia, no
conjunctival hemorrhage, and no discomfort on instillation.
Additionally, AKB-9778’s novel mechanism of action that targets the
Schlemm’s canal increases our excitement for this program and the
results we’ve seen to-date.”
The Phase 1b trial is a randomized, double-masked study designed
to assess increasing concentrations of AKB-9778 dosed topically as
eye drops. The primary outcome of the study is ocular safety and
tolerability with change in intraocular pressure (IOP) at Day 7 as
a pharmacodynamic outcome. Conjunctival hyperemia and IOP were
assessed at 0 (pre-dose), 2, 4, and 8 hours post-dose on Day -1
(baseline), Day 1 (first day of AKB-9778 dosing) and Day 7 (last
day of AKB-9778 dosing). Results from the first 3 cohorts, each
comprising 12 subjects with normotensive eyes (non-glaucoma
subjects), were reported on October 10, 2019. Subsequently, results
from cohort 4, also containing 12 subjects with normotensive eyes,
were observed to be consistent with those from cohorts 1 through
3.
Based on favorable tolerability and pharmacodynamic findings in
these ocular normotensive subjects from the first four cohorts,
Aerpio elected to recruit a fifth cohort of subjects with OHT/POAG
on standard of care prostaglandin therapy to assess the safety,
tolerability and pilot efficacy of once-daily AKB-9778 (40 mg/ml)
as an adjunctive therapy. In the fifth cohort 43 patients were
recruited with OHT/POAG and baseline IOP measurements between 17
and 27 mmHg while treated with once-daily prostaglandin therapy.
Patients were randomized 3:1 to receive either AKB-9778 (32
subjects) or placebo (11 subjects), administered in the morning for
7 days, while continuing their evening prostaglandin therapy.
Conjunctival hyperemia and IOP were assessed in the same manner as
described for cohorts 1-4.
About AKB-9778
AKB-9778 binds to and inhibits vascular endothelial protein
tyrosine phosphatase (VE-PTP), an important negative regulator of
Tie2. Decreased Tie2 activity contributes to vascular instability
in many diseases including diabetes. AKB-9778 activates the Tie2
receptor irrespective of extracellular levels of its binding
ligands, angiopoietin-1 (agonist) or angiopoietin-2 (antagonist)
and may be the most efficient pharmacologic approach to maintain
normal Tie2 activation.
About Aerpio Pharmaceuticals
Aerpio Pharmaceuticals, Inc. is a biopharmaceutical company
focused on advancing first-in-class compounds that activate Tie2 to
treat ocular diseases and complications of diabetes. Tie2 is an
important regulator of vascular stability, and its down-regulation,
through activation of two inhibitors VE-PTP and Ang-2, is found in
patients with diabetes and other conditions. The Company’s lead
compound, AKB-9778, a first-in-class small molecule inhibitor of
VE-PTP, is being investigated in an ongoing Phase 1b clinical trial
as a topical drop formulation for its therapeutic potential in
open-angle glaucoma. In the recently completed Phase 2b study
(TIME-2b) AKB-9778 demonstrated the ability to lower proteinuria
(as measured by decreasing urinary albumin creatine ratio, UACR) by
about 20% replicating a finding in the previous Phase 2 study. The
decrease in proteinuria suggests that AKB-9778 and our other Tie2
activating drug, ARP-1536, may have the potential to improve kidney
function in diabetics potentially delaying progression to kidney
dialysis. The Company’s second asset, ARP-1536 is a humanized
monoclonal antibody observed to activate Tie2 receptors in a
dose-dependent manner in preclinical models. Aerpio believes
ARP-1536 holds potential as a monthly or biweekly systemic therapy
to treat diabetic complications, including diabetic nephropathy.
The Company’s third asset is a bispecific antibody that binds both
VEGF and VE-PTP which inhibits VEGF activation and activates Tie2.
This bispecific antibody has the potential to be an improved
product for treating wet AMD and diabetic macular edema via
intravitreal injection. Finally, the Company has exclusively
out-licensed its fourth asset AKB-4924 (now called GB004), a
first-in-class small molecule inhibitor of hypoxia-inducible
factor-1 (HIF). GB004 is being developed by AKB-4924’s exclusive
licensor, Gossamer Bio, Inc. (Nasdaq: GOSS), in return for an
upfront payment of $20 million, future potential development,
regulatory, and sales milestones of up to $400 million, and
royalties on worldwide net sales. For more information, please
visit www.aerpio.com.
View source
version on businesswire.com: https://www.businesswire.com/news/home/20200207005534/en/
Investor & Media:
Aerpio Pharmaceuticals, Inc. Gina Marek VP of Finance
gmarek@aerpio.com
Aerpio Pharmaceuticals (NASDAQ:ARPO)
Historical Stock Chart
From Oct 2024 to Nov 2024
Aerpio Pharmaceuticals (NASDAQ:ARPO)
Historical Stock Chart
From Nov 2023 to Nov 2024