Matinas BioPharma reported revenue of $3.2 million for the year ended December 31, 2022, primarily from the BioNTech SE collaboration. The net loss attributable to common shareholders for 2022 was $21.0 million, or $0.10 per share. Cash, cash equivalents, and marketable securities as of December 31, 2022, were $28.8 million, expected to fund operations into the second quarter of 2024.
Near-term data readouts from internal and collaborative programs are expected to support the advancement of the LNC platform for delivery of nucleic acids.
FDA feedback from the MAT2203 Type B meeting is expected to impact partnership discussions and facilitate potential non-dilutive BARDA and/or NIH funding.
Phase 2 MAT2203 clinical trial results demonstrated the ability of the platform to efficaciously deliver a safe, well-tolerated oral form of amphotericin B with dramatic survival results.
The company is preparing to meet with the FDA to seek guidance on a Phase 3 study with MAT2203 for the treatment of invasive fungal infections.
Matinas BioPharma anticipates several milestones in the second quarter and second half of 2023, including data readouts from collaborations, progress in internal programs, and potential BARDA grant for MAT2203 development.