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Dyadic(DYAI) - 2024 Q3 - Earnings Call Transcript
DYAIDyadic(DYAI)2024-11-17 01:16

Financial Data and Key Metrics Changes - Revenue for Q3 2024 increased to approximately 1,958,000comparedto1,958,000 compared to 397,000 for the same period a year ago, driven by licensing revenue of 1millionfromProliantandasuccessfeeof1 million from Proliant and a success fee of 425,000 from Inzyme [38] - Cost of revenue for Q3 2024 increased to approximately 396,000comparedto396,000 compared to 106,000 for the same period a year ago, attributed to the increasing number of collaborations [39] - Research and development expenses decreased to approximately 460,000comparedto460,000 compared to 716,000 for the same period a year ago, reflecting the winding down of activities related to the Phase I clinical trial of DYAI-100 [40] - General and administrative expenses increased by 1.2% to 1,298,000comparedto1,298,000 compared to 1,282,000 for the same period a year ago [41] - Loss from operations decreased to 203,000comparedto203,000 compared to 1,720,000 for the same period a year ago, largely due to licensing revenue [42] - Net loss for Q3 2024 was 203,000or203,000 or 0.01 per share compared to 1,614,000or1,614,000 or 0.06 per share for the same period a year ago [43] Business Line Data and Key Metrics Changes - The focus on high-value alternative protein products is yielding tangible results, with significant progress in the commercialization of recombinant proteins like human serum albumin and alpha-lactalbumin [15][16] - The partnership with Proliant Health & Biologics is expected to generate significant revenue, with 1millionreceivedinaccessandmilestonefees[18]Thecompanyispreparingtolaunchitsownresearchgradeproducts,includingRNasefreeDNASE1,withpreordersexpectedtobegininearly2025[20][21]MarketDataandKeyMetricsChangesTheglobalcellculturemediamarketisvaluedatover1 million received in access and milestone fees [18] - The company is preparing to launch its own research-grade products, including RNase-free DNASE-1, with preorders expected to begin in early 2025 [20][21] Market Data and Key Metrics Changes - The global cell culture media market is valued at over 4.7 billion in 2023, expected to grow at a CAGR of 12.5% through 2030 [24] - The animal-free dairy products market is valued at over 26billionin2022,withongoingrevenuegenerationfromprecisionmicrobialfermentation[26]TheDNA/RNAenzymesmarketisestimatedat26 billion in 2022, with ongoing revenue generation from precision microbial fermentation [26] - The DNA/RNA enzymes market is estimated at 900 million, with plans to expand product offerings in this segment [22] Company Strategy and Development Direction - The company is pursuing a dual-track strategy focusing on near-term revenue from alternative proteins while building long-term value in human and animal health markets [31] - The strategic direction emphasizes the commercialization of alternative proteins and biopharmaceuticals, leveraging proprietary Dapibus and C1 platforms [13][14] - The company aims to capitalize on emerging opportunities in the health, wellness, and nutrition sectors, positioning itself as a leader in global protein production [13] Management's Comments on Operating Environment and Future Outlook - Management expressed confidence in the company's ability to meet current challenges and shape future solutions in health and nutrition [13] - The company is actively seeking non-dilutive pathways to advance development in avian influenza and Mpox vaccine candidates [88] - Management highlighted the importance of generating near-term revenue while building sustainable value through innovative solutions [88] Other Important Information - The company has cash and investment-grade securities of 10millionasofSeptember30,2024,comparedto10 million as of September 30, 2024, compared to 7.3 million as of December 31, 2023 [43] - Total cash burn for 2024 is expected to decrease significantly to approximately $4.7 million [43] Q&A Session Summary Question: Understanding regulatory requirements for research-grade recombinant proteins - Management clarified that manufacturing must be done at an ISO-certified facility, and there are no regulatory reviews needed for product launch, focusing on QA and QC specifications [45] Question: Number of certificates of analysis held - The company confirmed it has three certificates of analysis for DNASE-1, bovine transferrin, and bovine alpha-lactalbumin, all comparable to existing products [46] Question: Difficulty in manufacturing high-dollar research products - Management explained that production varies by market, with some products requiring high volumes while others are produced in smaller quantities, affecting profitability [50][51] Question: Market preference for recombinant versus animal-derived products - Management indicated that preferences depend on the application, with recombinant products generally preferred for their lower contamination risk [60][61] Question: Addressable market size and royalty rates - Management provided insights into the addressable market, estimating significant opportunities in cell culture media and DNA/RNA enzymes, with royalty rates varying by segment and application [66][70]