Aldeyra Therapeutics reported a net loss of $17.8 million for the three months ended June 30, 2022. The company's cash, cash equivalents, and marketable securities totaled $196.7 million as of June 30, 2022.
Pre-NDA meeting with the FDA scheduled for Q3 2022 to discuss NDA submission of Reproxalap for dry eye disease.
Pre-NDA meeting with the FDA planned for the second half of 2022 to discuss NDA submission of ADX-2191 for primary vitreoretinal lymphoma.
Top-line results from Phase 3 GUARD trial of ADX-2191 in proliferative vitreoretinopathy expected in the second half of 2022.
Top-line results from Phase 2 clinical trial of oral RASP modulator ADX-629 in acute alcoholic hepatitis expected in the second half of 2022.
Aldeyra believes that existing cash, cash equivalents, and marketable securities will be sufficient to fund currently projected operating expenses through the end of 2023.