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Xencor(XNCR) - 2022 Q2 - Earnings Call Transcript
XNCRXencor(XNCR)2022-08-04 03:28

Financial Data and Key Metrics Changes - Total revenue for Q2 2022 was 31million,andforthefirstsixmonths,itwas31 million, and for the first six months, it was 115.6 million, primarily from royalty revenue related to partnerships with Vir and Alexion [20][21] - Total cash equivalents, receivables, and marketable debt securities at June 30, 2022, totaled 679.7million,anincreaseofapproximately679.7 million, an increase of approximately 50 million from the beginning of the year [21][22] - The company updated its year-end guidance, estimating a cash balance between 550millionand550 million and 575 million by the end of 2022, sufficient to fund R&D programs through the end of 2025 [22] Business Line Data and Key Metrics Changes - The company has three royalty-producing marketed products, including ULTOMIRIS, which received a positive opinion from CHMP in Europe for generalized myasthenia gravis [8] - The company is advancing multiple clinical programs, including XmAb-564, plamotamab, and vudalimab, with data presentations planned through the end of the year [12][13][14] Market Data and Key Metrics Changes - The company is exploring external collaborations to enhance its technology for creating new drug molecules, exemplified by a partnership with Caris Life Sciences for target discovery [9] - The competitive landscape includes other companies like Amgen, which is advancing similar bispecific programs [18] Company Strategy and Development Direction - The company aims to utilize proof-of-concept data from early-stage studies to guide its development portfolio, focusing on programs with the greatest potential for success [6][7] - The modular approach and engineering tools allow the company to create a broad internal development portfolio in oncology and autoimmune diseases [6] Management's Comments on Operating Environment and Future Outlook - Management expressed confidence in the ability to avoid accessing public markets for capital for over four years due to revenue from strategic licensing and collaboration agreements [7] - The management highlighted the importance of differentiating their IL-15 assets from competitors, emphasizing a systemic therapy approach compared to local delivery methods [36][38] Other Important Information - The company is initiating a Phase I study of XmAb808, a CD28 targeting bispecific antibody, in combination with pembrolizumab [19] - The company is also exploring various immune indications for its IL-2 Fc program, with plans to disclose initial indications in the coming months [41] Q&A Session Summary Question: Can you talk about the B7-H3 target and its competitive landscape? - Management indicated that B7-H3 is a broadly expressed target across various solid tumor histologies and expressed no immediate concerns regarding recent adverse events reported by competitors [27][28] Question: What are the differentiating factors for your IL-15 assets compared to competitors? - The company highlighted that their IL-15 program is designed for systemic therapy, contrasting with a competitor's local delivery method, which may limit broader application [36][38] Question: How do you view the upcoming data readout for vudalimab? - Management noted that the initial data readout would be too early to draw conclusions about different patient subtypes but would provide insights into efficacy and tolerability [63] Question: What drove the increase in guidance for cash balance at year-end? - The increase was primarily attributed to higher-than-expected royalty revenue from partnerships, which provided more clarity on timing and amounts [108][109]