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Rigel(RIGL) - 2024 Q3 - Earnings Call Transcript
RIGLRigel(RIGL)2024-11-08 03:25

Financial Data and Key Metrics Changes - In Q3 2024, Rigel Pharmaceuticals reported total net sales of 38.9million,representinga4438.9 million, representing a 44% increase compared to Q3 2023 [9][52] - The company achieved a net income of 12.4 million in Q3 2024, compared to a net loss of 5.7millioninthesameperiodin2023[58]Cash,cashequivalents,andshortterminvestmentsincreasedto5.7 million in the same period in 2023 [58] - Cash, cash equivalents, and short-term investments increased to 61.1 million from 49.1million[58]BusinessLineDataandKeyMetricsChangesTAVALISSEgenerated49.1 million [58] Business Line Data and Key Metrics Changes - TAVALISSE generated 26.3 million in net product sales in Q3 2024, an 8% increase from 24.5millioninQ32023[52]REZLIDHIAachievednetproductsalesof24.5 million in Q3 2023 [52] - REZLIDHIA achieved net product sales of 5.5 million in Q3 2024, a 107% increase compared to 2.7millioninQ32023[52]GAVRETO,initsfirstfullquarter,generated2.7 million in Q3 2023 [52] - GAVRETO, in its first full quarter, generated 7.1 million in net product sales [52] Market Data and Key Metrics Changes - Rigel expanded its product presence outside the US with a new agreement with Kissei to develop and commercialize REZLIDHIA in Japan, Korea, and Taiwan, including a $10 million upfront payment [10] - The company shipped 2,793 bottles of TAVALISSE, 444 bottles of REZLIDHIA, and 752 bottles of GAVRETO in Q3 2024 [50][51] Company Strategy and Development Direction - Rigel's corporate strategy focuses on expanding its commercial portfolio, advancing its pipeline through collaborations and internal development, and maintaining financial discipline [8][63] - The company aims to become self-sustaining and reinvest in its development pipeline, with plans to discuss development plans for R289 and olutasidenib in 2025 [63] Management's Comments on Operating Environment and Future Outlook - Management expressed optimism about the company's growth trajectory, highlighting strong commercial execution and the successful transition of GAVRETO into Rigel's portfolio [14][60] - The company is well-positioned to continue driving value as it heads into 2025, with expectations for continued revenue growth [15][63] Other Important Information - Rigel is advancing the development of R289, a dual IRAK1/4 inhibitor, in a Phase 1b study for lower-risk MDS, with initial safety and efficacy data to be presented at the ASH meeting [11][32] - The company is exploring opportunities to in-license or acquire late-stage hematology and oncology assets to further expand its portfolio [13][35] Q&A Session Summary Question: Can you provide more color on TAVALISSE regarding the balance between refills and new prescriptions? - Management indicated that the majority of TAVALISSE's business comes from carryover, with growth from both new patient starts and existing patients [67][68] Question: What is the status of GAVRETO orders from top centers? - Management noted that a handful of top centers have not placed orders yet, but overall business through specialty pharmacies is improving [70][71] Question: How much of a stocking benefit was there during the initial phase of GAVRETO's launch? - Management clarified that the majority of Q3 sales were true demand, with some initial stocking contributing to sales figures [75][76] Question: What is the bar for success for R289 in lower-risk MDS? - Management expressed excitement about the data and indicated that the study is unique in enrolling relapsed/refractory patients, which could differentiate it from existing treatments [82][84] Question: How does Rigel's R289 compare to other IRAK inhibitors? - Management highlighted that R289 is a dual IRAK1 and 4 inhibitor, which may provide more profound inhibition of inflammatory cytokines compared to other single-target inhibitors [90]