Financial Data and Key Metrics - ZYNRELEF achieved a record net revenue of 5.6millioninQ42023,markingthefirsttimeitsurpassed5 million in a quarter [16] - The oncology franchise outperformed expectations with CINVANTI net revenues of 94.9millionandSUSTOLnetrevenuesof13 million for the year [25] - Total acute care net revenues for the year were 19.1million,includingAPONVIEnetrevenuesof1.4 million [55] - Gross margins improved to over 70% due to better inventory management and renegotiations with manufacturers, with future margins expected to reach the mid-70s range [24] - The company closed 2023 with over 80millionincashandcashequivalents,sufficienttoreachprofitabilitybyQ42024[24]BusinessLinePerformance−Theacutecarefranchise,particularlyZYNRELEF,isexpectedtodrivethemajorityofproductgrowth,withsignificantmomentumanticipatedin2025followingthelaunchofVANandfulltrainingofnewsalesrepresentatives[17]−Theoncologyfranchisecontinuestoshowconsistentperformance,withCINVANTIandSUSTOLexpectedtomaintaintheirstrongperformance[25]−APONVIEispositionedtoaddresspostoperativenauseaandvomiting,asignificantunmetneed,withhigh−riskpatientsexperiencingratesashighas80182 million in 2022 to 135 million in 2023 [53] - The label expansion for ZYNRELEF, approved by the FDA in January 2024, has doubled the number of indicated procedures, positioning it as a foundational element for postoperative analgesia [32] - The NOPAIN Act, effective from January 2025, will provide reimbursement for non-opioid products in outpatient surgical settings, further supporting the adoption of ZYNRELEF [33] Management Commentary on Operating Environment and Future Outlook - Management anticipates positive EBITDA by Q4 2024 and does not expect to raise additional capital, given the strong balance sheet and operational plan [70] - The company expects ZYNRELEF to see an inflection point in 2025, driven by the launch of VAN and the full impact of the CrossLink partnership [17] - The updated guidelines on postoperative nausea and vomiting prevention in 2024 are expected to enhance awareness and adoption of APONVIE [31] Other Important Information - The VAN (Vial Access Needle) project is progressing well, with expected approval by the end of 2024, and the Prefilled Syringe (PFS) is expected to be approved in 2026 [15] - The company has reduced SG&A expenses from 119.9 million in 2022 to 116.7 million in 2023, with further reductions anticipated [37] Q&A Session Summary Question: Impact of the NOPAIN Act on ZYNRELEF - The NOPAIN Act will provide reimbursement for ZYNRELEF in hospital outpatient departments and ASCs through 2027, with potential extension to 2030, ensuring broader adoption [74] Question: Cost Reduction Plans for 2024 - The company expects operating expenses to stabilize between 108 million to $160 million in 2024, with no significant further cost reductions anticipated [81] Question: Growth Expectations for ZYNRELEF in 2024 - Management remains comfortable with the 50% year-over-year growth projection for acute care products in 2024, driven by the CrossLink partnership and label expansion [76] Question: Opportunity in the ASC Segment - The ASC segment offers significant growth potential, particularly for ZYNRELEF and APONVIE, as the company focuses on the orthopedic space and aligns with ASC goals of rapid patient recovery [78]