SBIR/STTR Research Award

Novel injectable implants for long-term local controlled release of therapeutic monoclonal antibodies

Award identifier 31d8564f9a182a40cc1774ec54b0726d2a13e2a4d478d376ca21f860b1fbc2c6Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$350,027

Program and phase

SBIR · Phase I

Award year

2025

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
ASKO THERAPEUTICS, INC.
Proposal award date
2025-08-01
Contract end date
2026-07-31
UEI
HXZAWBGUS6X6
Solicitation number
PA24-245
Topic code
300

Research abstract

PROJECT SUMMARY/ABSTRACT Delivery of monoclonal antibody (mAb) therapeutics to hard-to-reach areas of the body such as the eye, brain, joint and tumor tissues suffer from low drug concentrations at the target tissue, systemic side effects, or frequent local injections. One established approach to overcome these issues is local and sustained drug exposure, achievable with locally injectable polymer long-acting release (LAR) implants, particularly those prepared from biocompatible and biodegradable poly (lactic-co-glycolic acid) (PLGA). PLGA has been used in > 25 FDA approved commercial LARs. MAbs are a growing drug class with important applications in local delivery such as age-related macular degeneration in the eye, osteoarthritis in joints and solid tumors in the brain, lung, and pancreas. However, development of injectable PLGA LARs for mAbs is complicated by the instability of the protein, particularly during microencapsulation and long-term drug release, and achieving desirable slow and continuous drug release over substantial durations (>1 month). Here, we propose to develop novel and injectable pencil lead-type PLGA implants that is capable of stably microencapsulating a variety of therapeutic MAbs while retaining desirable release kinetics of stabilized protein in vivo for 6-12 weeks in between injection. The technology exploits a combination of anhydrous protein encapsulation, control of microclimate pH in PLGA, and controlling high osmotic pressures induced by necessary stabilizing disaccharide excipients. This proposal will focus on formulation and optimization of sterile mAb/PLGA implants, using model mAbs of important clinical significance (anti-VEGF and anti-PD1), for constant delivery of commercial therapeutic antibodies. These formulations will be tested for their pharmacokinetics after a single injection and the implants will be assessed for mAb stability/release directly in vivo by implant recovery.

Technology keywords

Not reported

Other awards by this recipient

Verified by the same UEI. These are other public SBIR/STTR award pages, not a merged company record.

Awards with the same topic code

Verified by an exact topic code match. This is not a text-similarity match.

Research funding history

2 SBIR/STTR records share this UEI (2025). Reported award amounts total $700,054. Reported amounts are not federal obligations.

Phases: Phase I

Agencies: Department of Health and Human Services

Agency intelligence

Department of Health and Human Services

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