Elevation Oncology Reports Second Quarter 2024 Financial Results and Highlights Recent Business Achievements
Elevation Oncology (Nasdaq: ELEV) reported promising initial data from its Phase 1 clinical trial of EO-3021, showing a 42.8% confirmed ORR in Claudin 18.2-enriched gastric and GEJ cancer patients. The company is advancing to the dose expansion phase, with additional monotherapy data expected in 1H 2025. Elevation secured agreements with Lilly and GSK to evaluate EO-3021 in combination with ramucirumab and dostarlimab, respectively. The company remains on track to nominate a development candidate for its HER3-ADC program in 2H 2024.
Financially, Elevation reported $110.8 million in cash and equivalents as of June 30, 2024, up from $83.1 million at the end of 2023. Q2 2024 R&D expenses were $6.6 million, while G&A expenses were $4.4 million. The net loss for Q2 2024 was $10.5 million. The company expects its current cash position to fund operations into 2026.
Elevation Oncology (Nasdaq: ELEV) ha riportato dati iniziali promettenti dal suo trial clinico di Fase 1 per EO-3021, mostrando un 42,8% di tasso di risposta obiettiva confermata (ORR) nei pazienti con tumori gastrici e GEJ arricchiti di Claudin 18.2. L'azienda sta avanzando verso la fase di espansione delle dosi, con ulteriori dati sulla monoterapia attesi nel 1H 2025. Elevation ha raggiunto accordi con Lilly e GSK per valutare EO-3021 in combinazione rispettivamente con ramucirumab e dostarlimab. L'azienda prevede di nominare un candidato per lo sviluppo del suo programma HER3-ADC nel 2H 2024.
Dal punto di vista finanziario, Elevation ha riportato 110,8 milioni di dollari in contante e equivalenti a partire dal 30 giugno 2024, in aumento rispetto a 83,1 milioni di dollari alla fine del 2023. Le spese per R&S nel secondo trimestre del 2024 sono state di 6,6 milioni di dollari, mentre le spese generali e amministrative sono state di 4,4 milioni di dollari. La perdita netta per il secondo trimestre del 2024 è stata di 10,5 milioni di dollari. L'azienda prevede che la sua attuale posizione di cassa finanzierà le operazioni fino al 2026.
Elevation Oncology (Nasdaq: ELEV) reportó datos iniciales prometedores de su ensayo clínico de Fase 1 para EO-3021, mostrando una 42.8% de tasa de respuesta objetiva confirmada (ORR) en pacientes con cáncer gástrico y GEJ enriquecidos con Claudin 18.2. La empresa avanza hacia la fase de expansión de dosis, con datos adicionales de monoterapia esperados en 1H 2025. Elevation aseguró acuerdos con Lilly y GSK para evaluar EO-3021 en combinación con ramucirumab y dostarlimab, respectivamente. La compañía se mantiene en camino de nominar un candidato de desarrollo para su programa HER3-ADC en 2H 2024.
Desde el punto de vista financiero, Elevation reportó $110.8 millones en efectivo y equivalentes al 30 de junio de 2024, un aumento desde los $83.1 millones a finales de 2023. Los gastos de I+D del segundo trimestre de 2024 fueron de $6.6 millones, mientras que los gastos generales y administrativos fueron de $4.4 millones. La pérdida neta para el segundo trimestre de 2024 fue de $10.5 millones. La compañía espera que su posición de efectivo actual financie las operaciones hasta 2026.
Elevation Oncology (Nasdaq: ELEV)는 EO-3021의 1상 임상 시험에서 유망한 초기 데이터를 보고했으며, 콜루딘 18.2이 풍부한 위 및 GEJ 암 환자에서 42.8%의 확정된 객관적 반응률 (ORR)을 보였습니다. 이 회사는 용량 확장 단계로 진행 중이며, 2025년 1H에 추가 단독 치료 데이터를 기대하고 있습니다. Elevation은 각각 ramucirumab과 dostarlimab과의 조합으로 EO-3021을 평가하기 위해 Lilly 및 GSK와 계약을 체결했습니다. 이 회사는 HER3-ADC 프로그램에 대한 개발 후보를 2024년 하반기에 지명할 예정입니다.
재무적으로, Elevation은 2024년 6월 30일 기준으로 현금 및 현금 등가물로 $110.8 백만을 보고했으며, 이는 2023년 말의 $83.1 백만에서 증가한 수치입니다. 2024년 2분기 연구개발(R&D) 비용은 $6.6 백만이었고, 일반 관리(G&A) 비용은 $4.4 백만이었습니다. 2024년 2분기의 순손실은 $10.5 백만이었습니다. 이 회사는 현재 현금 위치로 2026년까지 운영을 자금 지원할 것으로 예상하고 있습니다.
Elevation Oncology (Nasdaq: ELEV) a rapporté des données initiales prometteuses de son essai clinique de phase 1 pour EO-3021, montrant un 42,8% de taux de réponse objective confirmée (ORR) chez des patients atteints de cancers gastriques et GEJ enrichis en Claudin 18.2. L'entreprise avance vers la phase d'expansion de dose, avec des données supplémentaires de monothérapie attendues au 1H 2025. Elevation a conclu des accords avec Lilly et GSK pour évaluer EO-3021 en combinaison avec le ramucirumab et le dostarlimab, respectivement. L'entreprise reste sur la bonne voie pour nommer un candidat de développement pour son programme HER3-ADC dans le 2H 2024.
Sur le plan financier, Elevation a rapporté 110,8 millions de dollars en liquidités et équivalents au 30 juin 2024, en hausse par rapport à 83,1 millions de dollars à la fin de 2023. Les dépenses de R&D du 2e trimestre 2024 étaient de 6,6 millions de dollars, tandis que les dépenses générales et administratives étaient de 4,4 millions de dollars. La perte nette pour le 2e trimestre 2024 s'élevait à 10,5 millions de dollars. L'entreprise s'attend à ce que sa position actuelle en liquidités finance ses opérations jusqu'en 2026.
Elevation Oncology (Nasdaq: ELEV) berichtete über vielversprechende erste Daten aus seiner klinischen Phase-1-Studie zu EO-3021, die eine 42,8% bestätigte objektive Ansprechraten (ORR) bei Patienten mit Claudin 18.2-angereichertem Magen- und GEJ-Krebs zeigen. Das Unternehmen schreitet zur Dosis-Erweiterungsphase voran, wobei zusätzliche Monotherapie-Daten im 1H 2025 erwartet werden. Elevation hat Vereinbarungen mit Lilly und GSK getroffen, um EO-3021 in Kombination mit Ramucirumab bzw. Dostarlimab zu evaluieren. Das Unternehmen ist auf Kurs, bis 2H 2024 einen Entwicklungs-Kandidaten für sein HER3-ADC-Programm zu nominieren.
Finanziell berichtete Elevation zum 30. Juni 2024 über 110,8 Millionen US-Dollar in Bar und Baräquivalenten, was einem Anstieg von 83,1 Millionen US-Dollar Ende 2023 entspricht. Die F&E-Ausgaben im 2. Quartal 2024 betrugen 6,6 Millionen US-Dollar, während die allgemeinen und Verwaltungsaufwendungen 4,4 Millionen US-Dollar betrugen. Der Nettoverlust im 2. Quartal 2024 betrug 10,5 Millionen US-Dollar. Das Unternehmen erwartet, dass seine aktuelle Barreserve die Operationen bis 2026 finanzieren wird.
- 42.8% confirmed ORR observed in Claudin 18.2-enriched subset of gastric and GEJ cancer patients
- EO-3021 demonstrated a differentiated safety profile with no neutropenia or peripheral neuropathy observed
- Secured clinical supply agreements with Lilly and GSK for combination studies
- Cash position increased to $110.8 million, expected to fund operations into 2026
- Raised $44.2 million through ATM facility in the first half of 2024
- Net loss increased to $10.5 million in Q2 2024 compared to $10.1 million in Q2 2023
- R&D expenses increased to $6.6 million in Q2 2024 from $6.0 million in Q2 2023
- G&A expenses rose to $4.4 million in Q2 2024 from $3.8 million in Q2 2023
Insights
The Q2 2024 results for Elevation Oncology show a mixed financial picture. While R&D expenses increased to
The net loss widened slightly to
The initial data from the Phase 1 trial of EO-3021 is highly promising. A
The planned combination studies with ramucirumab and dostarlimab are strategically sound, potentially enhancing efficacy. However, the
Elevation Oncology's focus on Claudin 18.2 and HER3 targets positions them well in the competitive ADC landscape. The initial EO-3021 data suggests potential for best-in-class status in Claudin 18.2-targeted therapies, a rapidly evolving field in oncology. The planned combinations with established drugs from Lilly and GSK demonstrate industry confidence in EO-3021's potential.
The company's pipeline diversification with the HER3-ADC program is strategically sound, given the growing interest in HER3 as a target. However, investors should note that while promising, these are still early-stage programs. The projected cash runway into 2026 provides a solid financial foundation for continued development, but future capital needs will depend on clinical progress and potential partnerships.
-- Today announced promising initial data from Phase 1 clinical trial of EO-3021;
-- Advancing into dose expansion portion of Phase 1 trial; additional monotherapy data expected in 1H 2025 --
-- Secured clinical supply agreements to evaluate EO-3021 in combination with ramucirumab and dostarlimab with Lilly and GSK, respectively; expect to initiate dosing in combination portion of the Phase 1 trial by year-end 2024 --
-- On-track to nominate development candidate for HER3-ADC program in 2H 2024 --
-- Elevation Oncology to host conference call and webcast today at 8:30 a.m. ET --
"Today, we announced promising initial data from our Phase 1 trial evaluating monotherapy EO-3021, which reinforce clinical proof-of-concept and support EO-3021's potential as a best-in-class Claudin 18.2 antibody drug conjugate. We are particularly excited to see encouraging anti-tumor activity in patients with Claudin 18.2-expressing gastric or GEJ cancer, as well as a differentiated safety profile, demonstrating the value of a targeted therapeutic approach and the benefit of EO-3021's site-specific conjugation," said Joseph Ferra, President and Chief Executive Officer of Elevation Oncology. "These results support our broad clinical development program for EO-3021 and strengthen our conviction that EO-3021 can provide meaningful benefit to patients living with gastric or GEJ cancer."
Mr. Ferra continued, "Looking ahead, we remain on track to advance into monotherapy dose expansion and initiate the combination portion of our Phase 1 trial evaluating EO-3021 by year-end, report additional monotherapy data for EO-3021 in the first half of 2025, and nominate a development candidate from our HER3-ADC program in the second half of 2024. This year has been transformative for Elevation Oncology, marked by strong execution toward our goal of bringing important treatment options to patients with significant unmet medical needs, and we are eager to continue these efforts as we advance our pipeline of differentiated ADC therapies."
Recent Business Achievements
- Earlier today, Elevation Oncology announced promising initial data from the dose escalation portion of the ongoing Phase 1 clinical trial of EO-3021 in patients with advanced, unresectable or metastatic solid tumors likely to express Claudin 18.2, including gastric, gastroesophageal junction (GEJ), pancreatic or esophageal cancers. As of the data cutoff date of June 10, 2024:
- EO-3021 was observed to be generally well-tolerated. No neutropenia or peripheral neuropathy/hypoesthesia, both known toxicities associated with monomethyl auristatin E (MMAE), were observed in the safety population of 32 patients treated with EO-3021.
- In seven patients with Claudin 18.2 in ≥
20% of tumor cells at IHC 2+/3+, the objective response rate (ORR) was42.8% (three confirmed partial responses, one of which was confirmed following the June 10, 2024, data cutoff) and the disease control rate (DCR) was71.4% , including two patients with stable disease (SD). - In eight patients with Claudin 18.2 in <
20% of tumor cells at IHC 2+/3+, the ORR was0% and the DCR was50% , including four patients with SD.
- A press release with further details regarding these results is available in the News Releases section of Elevation Oncology's investor relations website at https://investors.elevationoncology.com.
- In June 2024, Elevation Oncology announced plans to expand its ongoing Phase 1 clinical trial of EO-3021 to include two combination cohorts evaluating EO-3021 for the treatment of advanced gastric or GEJ cancer. Pursuant to clinical supply agreements with Lilly and Company and GSK, respectively, Elevation Oncology will evaluate EO-3021 in combination with ramucirumab, a VEGFR2 inhibitor, in the second-line setting and in combination with dostarlimab, a PD-1 inhibitor, in the front-line setting.
Expected Upcoming Milestones
EO-3021:
- Initiate dosing in combination portion of the ongoing Phase 1 clinical trial of EO-3021 by year-end 2024.
- Share additional data from the ongoing Phase 1 clinical trial of monotherapy EO-3021, including from the dose expansion cohort, in the first half of 2025.
HER3-ADC:
- Nominate development candidate from HER3-ADC program in the second half of 2024.
Second Quarter 2024 Financial Results
As of June 30, 2024, Elevation Oncology had cash, cash equivalents and marketable securities totaling
Research and development (R&D) expenses for the second quarter of 2024 were
General and administrative (G&A) expenses for the second quarter of 2024 were
Net loss for the second quarter of 2024 was
Financial Outlook
Elevation Oncology expects its existing cash, cash equivalents and marketable securities as of June 30, 2024 to be sufficient to fund its current operations into 2026.
Conference Call Information
Elevation Oncology will host a live conference call and webcast at 8:30 a.m. ET today to discuss the initial EO-3021 safety and efficacy data announced today. Participants may register for the conference call here. It is recommended that participants join the call ten minutes prior to the scheduled start.
A webcast of the call will also be available on the Events page of Elevation Oncology's investor relations website at https://investors.elevationoncology.com. The archived webcast will be available on the website approximately two hours after the conference call and will be available for 90 days following the call.
About EO-3021
EO-3021 (also known as SYSA1801) is a differentiated, clinical-stage antibody drug conjugate (ADC) with best-in-class potential comprised of an immunoglobulin G1 (IgG1) monoclonal antibody (mAb) that targets Claudin 18.2. EO-3021 is site-specifically conjugated to the monomethyl auristatin E (MMAE) payload via a cleavable linker with a drug-to-antibody ratio (DAR) of 2. Claudin 18.2 is a specific isoform of Claudin 18 that is normally expressed in gastric epithelial cells. During malignant transformation, the tight junctions may become disrupted, exposing Claudin 18.2 and allowing them to be accessible by Claudin 18.2 targeting agents. Elevation Oncology is evaluating EO-3021 in a Phase 1 study (NCT05980416) in patients with advanced, unresectable or metastatic solid tumors likely to express Claudin 18.2 including gastric, gastroesophageal junction, pancreatic or esophageal cancers.
Elevation Oncology has the exclusive rights to develop and commercialize EO-3021 in all global territories outside
About Elevation Oncology, Inc.
Elevation Oncology is an innovative oncology company focused on the discovery and development of selective cancer therapies to treat patients across a range of solid tumors with significant unmet medical needs. We are leveraging our antibody-drug conjugate (ADC) expertise to advance a novel pipeline, initially targeting two clinically validated targets in oncology, Claudin 18.2 and HER3. Our lead candidate, EO-3021, is a potential best-in-class ADC designed to target Claudin 18.2 and is currently being evaluated in a Phase 1 trial (NCT05980416) in patients with advanced, unresectable or metastatic solid tumors likely to express Claudin 18.2 including gastric, gastroesophageal junction, pancreatic or esophageal cancers. Additionally, we expect to nominate a development candidate for our second program, a HER3-targeting ADC for the treatment of patients with solid tumors that overexpress HER3, in 2024. For more information, visit www.ElevationOncology.com.
Forward-Looking Statements
This press release contains forward-looking statements within the meaning of the "safe harbor" provisions of the Private Securities Litigation Reform Act of 1995, including, but not limited to, anticipated clinical and preclinical development activities, expected timing of announcements of clinical results, potential benefits of Elevation Oncology's product candidates, potential market opportunities for Elevation Oncology's product candidates, the ability of Elevation Oncology's product candidates to treat their targeted indications and Elevation Oncology's expectations about its cash runway. All statements other than statements of historical fact are statements that could be deemed forward-looking statements. These forward-looking statements may be accompanied by such words as "aim," "anticipate," "believe," "could," "estimate," "expect," "forecast," "goal," "intend," "may," "might," "plan," "possible," "potential," "will," "would," and other words and terms of similar meaning. Although Elevation Oncology believes that the expectations reflected in such forward-looking statements are reasonable, Elevation Oncology cannot guarantee future events, results, actions, levels of activity, performance or achievements, and the timing and results of biotechnology development and potential regulatory approval are inherently uncertain. Forward-looking statements are subject to risks and uncertainties that may cause Elevation Oncology's actual activities or results to differ significantly from those expressed in any forward-looking statement, including risks and uncertainties related to Elevation Oncology's ability to advance its product candidates, the timing and results of preclinical studies and clinical trials, approvals and commercialization of product candidates, the receipt and timing of potential regulatory designations, Elevation Oncology's ability to fund development activities and achieve development goals, Elevation Oncology's ability to protect intellectual property, Elevation Oncology's ability to establish and maintain collaborations with third parties, and other risks and uncertainties described under the heading "Risk Factors" in documents Elevation Oncology files from time to time with the Securities and Exchange Commission. These forward-looking statements speak only as of the date of this press release, and Elevation Oncology undertakes no obligation to revise or update any forward-looking statements to reflect events or circumstances after the date hereof.
Elevation Oncology Investor and Media Contact
Hannah Deresiewicz, 212-362-1200
EVP, Managing Director, Precision AQ
hannah.deresiewicz@precisionaq.com
Selected Financial Information | ||||||
(In thousands, except share and per share data) | ||||||
(unaudited) | ||||||
Three months ended June 30, | ||||||
2024 | 2023 | |||||
Statement of Operations items: | ||||||
Operating expenses: | ||||||
Research and development | $ | 6,551 | $ | 6,029 | ||
General and administrative | 4,412 | 3,805 | ||||
Total operating expenses | 10,963 | 9,834 | ||||
Loss from operations | (10,963) | (9,834) | ||||
Other income (expense): | ||||||
Interest income (expense), net | 513 | (271) | ||||
Total other income (expense), net | 513 | (271) | ||||
Loss before income taxes | (10,450) | (10,105) | ||||
Income tax expense | 11 | 5 | ||||
Net loss | $ | (10,461) | $ | (10,110) | ||
Net loss per share, basic and diluted | $ | (0.18) | $ | (0.36) | ||
Weighted average common shares outstanding, basic and diluted | 59,018,340 | 28,405,046 |
Selected Financial Information | ||||||
(In thousands, except share and per share data) | ||||||
(unaudited) | ||||||
Selected Balance Sheet items: | June 30, 2024 | December 31, 2023 | ||||
Cash, cash equivalents and marketable securities | $ | 110,849 | $ | 83,107 | ||
Working capital1 | 110,806 | 83,819 | ||||
Total assets | 114,597 | 89,091 | ||||
Long-term debt, net of discount | 30,916 | 30,137 | ||||
Total stockholders' equity | 80,918 | 54,809 | ||||
1 We define working capital as current assets less current liabilities. |
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SOURCE Elevation Oncology
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