LUNA LABS USA LLC — Department of Health and Human Services SBIR Phase II: NICHD
LUNA LABS USA LLC — SBIR Phase II award from Department of Health and Human Services.
Phase II SBIR prototype / development signal
- Phase II is where Department of Health and Human Services funds deeper R&D after feasibility. Incumbents with Phase II history are serious competitors on adjacent topics.
- Use this award as past-performance context and to map customer organizations for STRATFI/TACFI-style transition planning.
- Obligated amount $750,687 is consistent with substantial Phase II-scale effort; compare to related awards from the same agency.
- Topic code NICHD links this award to a solicitation family — search the same topic stem for incumbents and recompete timing.
- Amount
- $750,687
- Agency
- Department of Health and Human Services · National Institutes of Health
- Program / Phase
- SBIR · Phase II
- Topic
- NICHD
- Solicitation
- PA22-176
- NAICS
- —
- Place of performance
- VA
- Period
- 2023-09-18 → 2025-08-31
Description
ABSTRACT An increased incidence of various pre-existing conditions like diabetes and hypertension, combined with systemic issues surrounding the quality of maternal health care provided, has resulted in a significant increase in the cesarean delivery rate in minority communities. These surgical procedures contribute to disparities in maternal health outcomes and postoperative complications, as C-sections increase the likelihood of pelvic adhesion formation. These adhesions are a leading cause of infertility, pain, and increased delivery time for subsequent births, and the disproportionate administration of these procedures in minority communities (i.e. these women are 33% more likely to undergo cesarean delivery) means these repercussions may be found more frequently in these populations. Current products for adhesion prevention are difficult to apply in gynecologic procedures and fail to properly address this severe surgical complication. Luna Labs’ patented AeroVeil technology, a two-component sprayable hydrogel, has been demonstrated effective in decreasing the incidence and severity of abdominal adhesion formation in rat and rabbit models. The proposed program will focus on transitioning product application from these abdominal adhesion models into wound healing and efficacy models of gynecologic applications to evaluate the safety and efficacy of product application in this space. Successful completion of these efforts will drive technology transition and regulatory approval to support the initiation of clinical trials with a commercial partner and reduce the needless surgical complications suffered by women in minority communities.