ORIC Pharmaceuticals Reports Second Quarter 2024 Financial Results and Operational Updates
ORIC Pharmaceuticals reported Q2 2024 financial results and operational updates. Key highlights include:
- Initiated ORIC-944 dosing in combinations with NUBEQA® and ERLEADA® in an ongoing Phase 1b prostate cancer trial
- Entered clinical trial collaboration agreements with Bayer and Johnson & Johnson
- Appointed Keith Lui as SVP of Commercial and Medical Affairs
- Cash and investments of $308.5 million, expected to fund operations into late 2026
- R&D expenses increased to $28.9 million in Q2 2024, up from $18.8 million in Q2 2023
- G&A expenses rose to $7.1 million in Q2 2024, compared to $6.2 million in Q2 2023
The company progressed its pipeline, including ORIC-114 for NSCLC and ORIC-944 for prostate cancer, with data updates expected in 2025.
ORIC Pharmaceuticals ha riportato i risultati finanziari e gli aggiornamenti operativi per il secondo trimestre del 2024. I punti salienti includono:
- Iniziata la somministrazione di ORIC-944 in combinazione con NUBEQA® e ERLEADA® in un attuale studio clinico di fase 1b per il cancro alla prostata
- Stipulati accordi di collaborazione per studi clinici con Bayer e Johnson & Johnson
- Nominato Keith Lui come SVP delle Attività Commerciali e Mediche
- Cassa e investimenti pari a $308,5 milioni, previsti per finanziare le operazioni fino alla fine del 2026
- Le spese per R&S sono aumentate a $28,9 milioni nel secondo trimestre del 2024, rispetto ai $18,8 milioni del secondo trimestre del 2023
- Le spese generali e amministrative sono salite a $7,1 milioni nel secondo trimestre del 2024, rispetto ai $6,2 milioni del secondo trimestre del 2023
La società ha fatto progressi nel suo pipeline, compresi ORIC-114 per il NSCLC e ORIC-944 per il cancro alla prostata, con aggiornamenti dei dati attesi nel 2025.
ORIC Pharmaceuticals informó sobre los resultados financieros y las actualizaciones operativas del segundo trimestre de 2024. Los aspectos destacados incluyen:
- Se inició la dosificación de ORIC-944 en combinaciones con NUBEQA® y ERLEADA® en un ensayo clínico de fase 1b para el cáncer de próstata
- Se firmaron acuerdos de colaboración para ensayos clínicos con Bayer y Johnson & Johnson
- Se nombró a Keith Lui como SVP de Asuntos Comerciales y Médicos
- Liquidaciones e inversiones de $308,5 millones, se espera que financien las operaciones hasta finales de 2026
- Los gastos de I+D se incrementaron a $28,9 millones en el segundo trimestre de 2024, frente a los $18,8 millones en el segundo trimestre de 2023
- Los gastos generales y administrativos aumentaron a $7,1 millones en el segundo trimestre de 2024, en comparación con los $6,2 millones en el segundo trimestre de 2023
La empresa avanzó en su pipeline, incluyendo ORIC-114 para NSCLC y ORIC-944 para cáncer de próstata, con actualizaciones de datos esperadas para 2025.
ORIC Pharmaceuticals는 2024년 2분기 재무 결과 및 운영 업데이트를 보고했습니다. 주요 내용은 다음과 같습니다:
- 현재 진행 중인 1b상 전립선암 임상 시험에서 NUBEQA® 및 ERLEADA®와 병용한 ORIC-944 용량을 시작했습니다.
- Bayer 및 Johnson & Johnson과 임상 시험 협력 계약을 체결했습니다.
- Keith Lui를 상업 및 의료 업무의 SVP로 임명했습니다.
- 현금 및 투자금이 $3억 8천 5백만 달러로, 2026년 말까지 운영 자금을 지원할 것으로 예상됩니다.
- 2024년 2분기 R&D 비용이 $2천 8백 9십만 달러로 증가했으며, 이는 2023년 2분기의 $1천 8백 8십만 달러에서 증가한 것입니다.
- 2024년 2분기 G&A 비용이 $7백 10만 달러로 증가했으며, 이는 2023년 2분기의 $6백 2십만 달러에 비해 증가한 것입니다.
회사는 NSCLC용 ORIC-114 및 전립선암용 ORIC-944를 포함한 파이프라인을 발전시켰으며, 2025년 데이터 업데이트가 예상됩니다.
ORIC Pharmaceuticals a annoncé les résultats financiers et les mises à jour opérationnelles du deuxième trimestre 2024. Les points saillants comprennent :
- Démarrage de l'administration de ORIC-944 en combinaison avec NUBEQA® et ERLEADA® dans un essai clinique de phase 1b sur le cancer de la prostate en cours
- Conclusion d'accords de collaboration pour des essais cliniques avec Bayer et Johnson & Johnson
- Nommer Keith Lui au poste de SVP des affaires commerciales et médicales
- Un fonds de $308,5 millions, prévu pour financer les opérations jusqu'à fin 2026
- Les dépenses de R&D ont augmenté à $28,9 millions au Q2 2024, contre $18,8 millions au Q2 2023
- Les dépenses générales et administratives ont augmenté à $7,1 millions au Q2 2024, contre $6,2 millions au Q2 2023
L'entreprise a progressé dans son pipeline, y compris ORIC-114 pour le NSCLC et ORIC-944 pour le cancer de la prostate, avec des mises à jour des données attendues en 2025.
ORIC Pharmaceuticals hat die finanziellen Ergebnisse und betrieblichen Updates für das zweite Quartal 2024 veröffentlicht. Zu den wichtigsten Punkten gehören:
- Beginn der Dosierung von ORIC-944 in Kombination mit NUBEQA® und ERLEADA® in einer laufenden Phase-1b-Studie zum Prostatakrebs
- Abschluss von klinischen Studien-Kooperationsvereinbarungen mit Bayer und Johnson & Johnson
- Keith Lui als SVP für kommerzielle und medizinische Angelegenheiten ernannt
- Barmittel und Investitionen von $308,5 Millionen, die voraussichtlich die Betriebe bis Ende 2026 finanzieren werden
- Die Forschungs- und Entwicklungskosten erhöhten sich im Q2 2024 auf $28,9 Millionen, gegenüber $18,8 Millionen im Q2 2023
- Die allgemeinen und administrativen Aufwendungen stiegen im Q2 2024 auf $7,1 Millionen, verglichen mit $6,2 Millionen im Q2 2023
Das Unternehmen hat seinen Produktpipeline vorangetrieben, einschließlich ORIC-114 für NSCLC und ORIC-944 für Prostatakrebs, mit Datenupdates, die für 2025 erwartet werden.
- Initiated dosing of ORIC-944 in combinations with NUBEQA® and ERLEADA® in ongoing Phase 1b prostate cancer trial
- Entered clinical trial collaboration agreements with Bayer and Johnson & Johnson
- Cash and investments of $308.5 million, expected to fund operations into late 2026
- Expanded leadership team with appointment of Keith Lui as SVP of Commercial and Medical Affairs
- Completed dose escalation and selected two provisional recommended phase 2 doses for ORIC-114
- R&D expenses increased by $10.2 million to $28.9 million in Q2 2024 compared to Q2 2023
- G&A expenses increased by $0.9 million to $7.1 million in Q2 2024 compared to Q2 2023
Insights
ORIC Pharmaceuticals' Q2 2024 results show a strong financial position with
ORIC's progress in oncology drug development is noteworthy. The advancement of ORIC-114, a brain-penetrant EGFR/HER2 inhibitor, into expansion cohorts for various NSCLC subtypes is promising. The initiation of combination dosing for ORIC-944 with established prostate cancer treatments like NUBEQA® and ERLEADA® could potentially enhance efficacy. The preclinical data on ORIC-613, targeting PLK4, adds depth to their pipeline. These developments, coupled with strategic collaborations with major pharma companies, position ORIC well in the competitive oncology space. The focus on addressing mechanisms of therapeutic resistance is a critical approach in improving cancer treatment outcomes.
ORIC's strategic moves in Q2 2024 demonstrate a well-rounded approach to drug development and commercialization. The expansion of the leadership team with Keith Lui's appointment signals preparation for potential product launches. The clinical trial collaborations with Bayer and Johnson & Johnson not only provide supply support but also validate ORIC's approach and could lead to future partnerships. The company's focus on multiple cancer types and mechanisms of resistance diversifies risk. With multiple data readouts expected in 2025 and potential initiation of registrational trials, ORIC is positioning itself for significant near-term catalysts that could drive value for investors.
Initiated dosing of ORIC-944 in combinations with NUBEQA® (darolutamide) and ERLEADA® (apalutamide) in the ongoing Phase 1b trial for prostate cancer
Entered into clinical trial collaboration and supply agreements with Bayer and Johnson & Johnson to support the ongoing Phase 1b trial of ORIC-944 in combination with NUBEQA® and in combination with ERLEADA®
Expanded leadership team with the appointment of industry veteran Keith Lui as Senior Vice President of Commercial and Medical Affairs
Cash and investments of
SOUTH SAN FRANCISCO, Calif. and SAN DIEGO, Aug. 12, 2024 (GLOBE NEWSWIRE) -- ORIC Pharmaceuticals, Inc. (Nasdaq: ORIC), a clinical stage oncology company focused on developing treatments that address mechanisms of therapeutic resistance, today reported financial results and operational updates for the quarter ended June 30, 2024.
“We have made strong progress on advancing the pipeline, deepening strategic relationships, and growing the leadership team to add new functional capabilities,” said Jacob M. Chacko, M.D., president and chief executive officer. “We are making good progress on the expansion cohorts for ORIC-114 in three different selected patient populations in NSCLC and have initiated combination dosing for ORIC-944 in prostate cancer. The clinical trial collaboration and supply agreements with Bayer and Johnson & Johnson are pivotal steps in supporting those combination cohorts. Finally, we bolstered our leadership team to add commercial and medical affairs capabilities in advance of the potential initiation of multiple registrational trials in 2025. We look forward to sharing further clinical updates in 2025.”
Second Quarter 2024 and Other Recent Highlights
ORIC-114: a brain penetrant, orally bioavailable, irreversible EGFR/HER2 inhibitor
- Announced the completion of the dose escalation portion of the Phase 1b trial of ORIC-114 and the selection of two provisional recommended phase 2 doses.
- Announced first patients dosed across three expansion cohorts in the Phase 1b trial of ORIC-114 in patients with mutated non-small cell lung cancer (NSCLC), including EGFR exon 20 insertion (EGFR exon 20 inhibitor naïve), HER2 exon 20 insertion, and EGFR atypical mutations.
- Initiated an extension cohort to evaluate ORIC-114 for the treatment of patients with first-line, treatment-naïve EGFR exon 20 insertion NSCLC.
- Expect to report updated Phase 1b data in the first half of 2025.
ORIC-944: a potent and selective allosteric inhibitor of PRC2
- Initiated dosing of ORIC-944 in combination with NUBEQA® (darolutamide) and in combination with ERLEADA® (apalutamide) in the ongoing Phase 1b trial for prostate cancer in first half of 2024.
- Entered into clinical trial collaboration and supply agreements with Bayer and Johnson & Johnson to support the ongoing Phase 1b trial of ORIC-944 in combinations with AR inhibitors for the treatment of prostate cancer.
- Presented preclinical data at the 2024 AACR Annual Meeting demonstrating superior drug properties and synergy data in prostate cancer models, reinforcing the promise of ORIC-944 as a potential best-in-class treatment for combination with AR inhibitors.
Discovery Pipeline:
- Presented at the 2024 AACR annual meeting the first preclinical data on ORIC-613, a potential first- and best-in-class development candidate selectively inhibiting PLK4.
Corporate Highlights:
- Expanded the leadership team with the appointment of industry veteran Keith Lui as Senior Vice President of Commercial and Medical Affairs.
Second Quarter 2024 Financial Results
- Cash, Cash Equivalents and Investments: Cash, cash equivalents and investments totaled
$308.5 million as of June 30, 2024, which the company expects will be sufficient to fund its operating plan into late 2026.
- R&D Expenses: Research and development (R&D) expenses were
$28.9 million for the three months ended June 30, 2024, compared to$18.8 million for the three months ended June 30, 2023, an increase of$10.2 million . For the six months ended June 30, 2024, R&D expenses were$50.9 million , compared to$38.3 million for the six months ended June 30, 2023, an increase of$12.6 million . The increases were due to a net increase in external expenses related to the advancement of product candidates and discovery programs, as well as higher personnel costs, including additional non-cash stock-based compensation of$0.6 million and$1.2 million for the three and six months ended June 30, 2024, respectively.
- G&A Expenses: General and administrative (G&A) expenses were
$7.1 million for the three months ended June 30, 2024, compared to$6.2 million for the three months ended June 30, 2023, an increase of$0.9 million . For the six months ended June 30, 2024, G&A expenses were$14.1 million , compared to$12.4 million for the six months ended June 30, 2023, an increase of$1.7 million . The increases were primarily due to higher personnel costs, including additional non-cash stock-based compensation of$0.6 million and$1.3 million for the three and six months ended June 30, 2024, respectively.
About ORIC Pharmaceuticals, Inc.
ORIC Pharmaceuticals is a clinical stage biopharmaceutical company dedicated to improving patients’ lives by Overcoming Resistance In Cancer. ORIC’s clinical stage product candidates include (1) ORIC-114, a brain penetrant inhibitor designed to selectively target EGFR and HER2 with high potency against exon 20 insertion mutations, being developed across multiple genetically defined cancers, (2) ORIC-944, an allosteric inhibitor of the polycomb repressive complex 2 (PRC2) via the EED subunit, being developed for prostate cancer, and (3) ORIC-533, an orally bioavailable small molecule inhibitor of CD73, a key node in the adenosine pathway believed to play a central role in resistance to chemotherapy- and immunotherapy-based treatment regimens, being developed for multiple myeloma. Beyond these three product candidates, ORIC® is also developing multiple precision medicines targeting other hallmark cancer resistance mechanisms. ORIC has offices in South San Francisco and San Diego, California. For more information, please go to www.oricpharma.com, and follow us on X or LinkedIn.
Cautionary Note Regarding Forward-Looking Statements
This press release contains forward-looking statements as that term is defined in Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934. Statements in this press release that are not purely historical are forward-looking statements. Such forward-looking statements include, among other things, statements regarding the continued clinical development of ORIC-114 and ORIC-944; ORIC-114 clinical outcomes, which may materially change as patient enrollment continues or more patient data become available; the development plans and timelines for ORIC-114, ORIC-944 and ORIC’s other product candidates; the potential advantages of ORIC-114, ORIC-944 and ORIC’s other product candidates and programs; plans underlying ORIC’s clinical trials and development; anticipated program milestones, including timing of program and data updates and the initiation of registrational studies; the period over which ORIC estimates its existing cash, cash equivalents and investments will be sufficient to fund its current operating plan; and statements by the company’s chief executive officer. Words such as “believes,” “anticipates,” “plans,” “expects,” “intends,” “will,” “goal,” “potential” and similar expressions are intended to identify forward-looking statements. The forward-looking statements contained herein are based upon ORIC’s current expectations and involve assumptions that may never materialize or may prove to be incorrect. Actual results could differ materially from those projected in any forward-looking statements due to numerous risks and uncertainties, including but not limited to: risks associated with the process of discovering, developing and commercializing drugs that are safe and effective for use as human therapeutics and operating as an early clinical stage company; ORIC’s ability to develop, initiate or complete preclinical studies and clinical trials for, obtain approvals for and commercialize any of its product candidates; changes in ORIC’s plans to develop and commercialize its product candidates; the potential for clinical trials of ORIC’s product candidates to differ from preclinical, initial, interim, preliminary or expected results; negative impacts of health emergencies, economic instability or international conflicts on ORIC’s operations, including clinical trials; the risk of the occurrence of any event, change or other circumstance that could give rise to the termination of ORIC’s license and collaboration agreements or its clinical trial collaboration and supply agreements; the potential market for ORIC’s product candidates, and the progress and success of competing therapeutics currently available or in development; ORIC’s ability to raise any additional funding it will need to continue to pursue its business and product development plans; regulatory developments in the United States and foreign countries; ORIC’s reliance on third parties, including contract manufacturers and contract research organizations; ORIC’s ability to obtain and maintain intellectual property protection for its product candidates; the loss of key scientific or management personnel; competition in the industry in which ORIC operates; general economic and market conditions; and other risks. Information regarding the foregoing and additional risks may be found in the section titled “Risk Factors” in ORIC’s Quarterly Report on Form 10-Q filed with the Securities and Exchange Commission (the “SEC”) on August 12, 2024, and ORIC’s future reports to be filed with the SEC. These forward-looking statements are made as of the date of this press release, and ORIC assumes no obligation to update the forward-looking statements, or to update the reasons why actual results could differ from those projected in the forward-looking statements, except as required by law.
Contact:
Dominic Piscitelli, Chief Financial Officer
dominic.piscitelli@oricpharma.com
info@oricpharma.com
ORIC PHARMACEUTICALS, INC. CONDENSED BALANCE SHEETS (in thousands, except share and per share amounts) | |||||||
June 30, 2024 | December 31, 2023 | ||||||
(unaudited) | |||||||
Assets | |||||||
Current assets: | |||||||
Cash, cash equivalents and short-term investments | $ | 286,406 | $ | 208,187 | |||
Prepaid expenses and other current assets | 8,193 | 4,410 | |||||
Total current assets | 294,599 | 212,597 | |||||
Long-term investments | 22,126 | 26,852 | |||||
Property and equipment, net | 2,878 | 2,862 | |||||
Other assets | 9,303 | 9,696 | |||||
Total assets | $ | 328,906 | $ | 252,007 | |||
Liabilities and Stockholders' Equity | |||||||
Current liabilities: | |||||||
Accounts payable | $ | 2,309 | $ | 944 | |||
Accrued liabilities | 17,230 | 19,514 | |||||
Total current liabilities | 19,539 | 20,458 | |||||
Other long-term liabilities | 6,967 | 7,461 | |||||
Total liabilities | 26,506 | 27,919 | |||||
Total stockholders' equity | 302,400 | 224,088 | |||||
Total liabilities and stockholders' equity | $ | 328,906 | $ | 252,007 |
ORIC PHARMACEUTICALS, INC. STATEMENTS OF OPERATIONS AND COMPREHENSIVE LOSS (Unaudited) (in thousands, except share and per share amounts) | |||||||||||||||
Three Months Ended June 30, | Six Months Ended June 30, | ||||||||||||||
2024 | 2023 | 2024 | 2023 | ||||||||||||
Operating expenses: | |||||||||||||||
Research and development | $ | 28,940 | $ | 18,787 | $ | 50,900 | $ | 38,303 | |||||||
General and administrative | 7,077 | 6,205 | 14,107 | 12,367 | |||||||||||
Total operating expenses | 36,017 | 24,992 | 65,007 | 50,670 | |||||||||||
Loss from operations | (36,017 | ) | (24,992 | ) | (65,007 | ) | (50,670 | ) | |||||||
Other income, net | 4,054 | 2,048 | 8,033 | 3,781 | |||||||||||
Net loss | $ | (31,963 | ) | $ | (22,944 | ) | $ | (56,974 | ) | $ | (46,889 | ) | |||
Other comprehensive (loss) income: | |||||||||||||||
Unrealized (loss) gain on investments | (94 | ) | (68 | ) | (514 | ) | 724 | ||||||||
Comprehensive loss | $ | (32,057 | ) | $ | (23,012 | ) | $ | (57,488 | ) | $ | (46,165 | ) | |||
Net loss per share, basic and diluted | $ | (0.45 | ) | $ | (0.50 | ) | $ | (0.83 | ) | $ | (1.03 | ) | |||
Weighted-average shares outstanding, basic and diluted | 70,348,414 | 45,654,208 | 68,848,981 | 45,373,745 |
FAQ
What were ORIC Pharmaceuticals' Q2 2024 financial results?
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