Foghorn Therapeutics Provides Third Quarter 2024 Financial and Corporate Update
Foghorn Therapeutics reports Q3 2024 financial results and pipeline updates. Key highlights include: First patient dosed with FHD-909 in Phase 1 trial for SMARCA4 mutated NSCLC; Topline Phase 1 data for FHD-286 plus decitabine in AML expected by year-end 2024; IND-enabling studies for Selective CBP degrader program to begin by year-end. Financial position: $267.4M cash runway into 2027; Q3 revenue at $7.8M (down from $17.5M in Q3 2023); Net loss increased to $19.1M from $14.3M year-over-year.
Foghorn Therapeutics ha riportato i risultati finanziari del terzo trimestre 2024 e aggiornamenti sul proprio pipeline. I punti salienti includono: Primo paziente trattato con FHD-909 in fase 1 dello studio per il carcinoma polmonare non a piccole cellule con mutazione SMARCA4; I dati preliminari della fase 1 per FHD-286 più decitabina in AML sono attesi entro la fine del 2024; Gli studi per abilitare l'IND del programma di degradatori selettivi di CBP inizieranno entro la fine dell'anno. Posizione finanziaria: $267,4M di liquidità fino al 2027; Fatturato del terzo trimestre di $7,8M (in calo rispetto ai $17,5M del terzo trimestre 2023); La perdita netta è aumentata a $19,1M rispetto ai $14,3M dell'anno precedente.
Foghorn Therapeutics reporta los resultados financieros del tercer trimestre de 2024 y actualizaciones de su cartera de productos. Los aspectos destacados incluyen: Primer paciente tratado con FHD-909 en el ensayo de fase 1 para cáncer de pulmón no microcítico mutado por SMARCA4; Los datos preliminares de fase 1 para FHD-286 más decitabina en AML se esperan para finales de 2024; Los estudios que habilitan el IND para el programa de degradadores selectivos de CBP comenzarán para finales del año. Situación financiera: $267,4M de efectivo disponible hasta 2027; Ingresos del tercer trimestre de $7,8M (bajando de $17,5M en el tercer trimestre de 2023); La pérdida neta aumentó a $19,1M desde $14,3M en comparación con el año anterior.
Foghorn Therapeutics는 2024년 3분기 재무 결과와 파이프라인 업데이트를 보고했습니다. 주요 사항은 다음과 같습니다: SMARCA4 변이가 있는 비소세포폐암에 대한 1상 시험에서 첫 번째 환자가 FHD-909로 투여됨; 2024년 연말까지 AML에서 FHD-286과 데시타빈에 대한 1상 데이터 발표 예정; 선택적 CBP 분해제 프로그램을 위한 IND 승인 가능 연구가 연말까지 시작될 예정입니다. 재무 상황: 2027년까지 사용할 수 있는 현금이 $267.4M; 3분기 수익은 $7.8M(2023년 3분기 $17.5M에서 감소); 순손실은 지난해 $14.3M에서 증가한 $19.1M에 달했습니다.
Foghorn Therapeutics rapporte les résultats financiers du troisième trimestre 2024 et des mises à jour sur son pipeline. Les faits saillants incluent : Premier patient traité avec FHD-909 dans un essai de phase 1 pour le NSCLC muté SMARCA4; Les données préliminaires de la phase 1 pour FHD-286 plus de la décitabine dans l'AML sont attendues d'ici la fin de 2024; Les études permettant d'obtenir l'IND pour le programme de dégradeurs sélectifs de CBP devraient commencer d'ici la fin de l'année. Situation financière: 267,4 millions de dollars de liquidités jusqu'en 2027; Chiffre d'affaires du troisième trimestre de 7,8 millions de dollars (en baisse par rapport à 17,5 millions de dollars au troisième trimestre 2023); La perte nette a augmenté de 14,3 millions de dollars l'année précédente à 19,1 millions de dollars.
Foghorn Therapeutics berichtet über die finanziellen Ergebnisse des dritten Quartals 2024 und Updates zum Pipeline. Wichtige Highlights sind: Erster Patient mit FHD-909 in der Phase-1-Studie für SMARCA4-mutativen NSCLC behandelt; Die vorläufigen Phase-1-Daten für FHD-286 in Kombination mit Decitabin bei AML werden bis Ende 2024 erwartet; IND-erlaubende Studien für das selektive CBP-Abbauprogramm werden bis Ende des Jahres beginnen. Finanzielle Lage: $267,4M Cash-Reserve bis 2027; Einnahmen im dritten Quartal betrugen $7,8M (Rückgang von $17,5M im dritten Quartal 2023); Der Nettoverlust stieg im Jahresvergleich von $14,3M auf $19,1M.
- Strong cash position of $267.4M providing runway into 2027
- First patient dosed in Phase 1 trial for FHD-909 in SMARCA4 mutated NSCLC
- Strategic collaboration with Lilly includes 50/50 co-development agreement
- Revenue decreased to $7.8M from $17.5M in Q3 2023
- Net loss increased to $19.1M from $14.3M year-over-year
- End of Merck collaboration in August 2023 impacting revenue
Insights
The Q3 update reveals significant clinical progress and strong financial positioning. The initiation of FHD-909's Phase 1 trial targeting SMARCA4-mutated NSCLC represents a major milestone in precision oncology. With approximately
The robust cash position of
Key catalysts include the upcoming FHD-286 combination therapy data in AML by year-end and the advancement of the CBP degrader program to IND-enabling studies. The pipeline's focus on synthetic lethality and protein degradation represents cutting-edge approaches in oncology.
The financial position shows strong fiscal management with a healthy balance sheet. The
The reduction in operating expenses, particularly the
First patient dosed with first-in-class SMARCA2(BRM) selective inhibitor FHD-909 (LY4050784) in Phase 1 trial with primary target population in SMARCA4(BRG1) mutated NSCLC
Topline Phase 1 dose escalation data for FHD-286 plus decitabine in patients with relapsed and/or refractory AML expected by year-end 2024
IND-enabling studies for Selective CBP degrader program on track to begin by year-end 2024
Strong balance sheet with cash, cash equivalents, and marketable securities of
CAMBRIDGE, Mass., Nov. 04, 2024 (GLOBE NEWSWIRE) -- Foghorn® Therapeutics Inc. (Nasdaq: FHTX), a clinical-stage biotechnology company pioneering a new class of medicines that treat serious diseases by correcting abnormal gene expression, today provided a financial and corporate update in conjunction with the Company’s 10-Q filing for the quarter ended September 30, 2024. With an initial focus in oncology, Foghorn’s Gene Traffic Control® Platform and resulting broad pipeline have the potential to transform the lives of people suffering from a wide spectrum of diseases.
“We continue to advance our pipeline of multiple therapeutics targeting novel biology in the chromatin regulatory system. The first patient was recently dosed with FHD-909, a highly selective SMARCA2 (BRM) inhibitor, that targets the SMARCA2 synthetic lethal relationship with SMARCA4 (BRG1) mutated NSCLC. We look forward to further clinical progress with the FHD-909 program in collaboration with our partner Lilly,” said Adrian Gottschalk, President and Chief Executive Officer of Foghorn. “By year-end, we expect data from our FHD-286 combination study in AML and expect to initiate IND-enabling studies for our Selective CBP degrader program targeting tumors harboring EP300 mutations, including bladder, gastric, and endometrial cancers. With our strong cash position and runway into 2027, we are poised to advance our clinical and preclinical pipeline.”
Recent Corporate Updates
Presented at 7th Annual Targeted Protein Degradation (TPD) Summit. In October, Foghorn participated in multiple sessions at the 7th Annual TPD Summit, including a CEO Think Tank keynote session entitled "A Strategic Look at Targeted Protein Degradation & Induced Proximity Field" featuring Foghorn’s CEO Adrian Gottschalk, and a presentation by Steve Bellon, Foghorn’s Chief Scientific Officer, on the recent developments from Foghorn’s degrader pipeline.
Dosed First Patient with FHD-909. In October, the first patient was dosed with FHD-909 in the Phase 1 open-label, multicenter trial for SMARCA4 mutated cancers, with non-small cell lung cancer (NSCLC) as the primary target patient population.
Strengthened Executive Leadership. In September, Foghorn appointed Anna Rivkin, Ph.D., as Chief Business Officer. Dr. Rivkin brings over two decades of expertise establishing strategic alliances, R&D partnerships, in-licensing and M&A. Most recently, she held leadership roles at Bristol Myers Squibb where she successfully oversaw a broad range of complex business transactions across multiple disease areas.
Program Overview and Upcoming Milestones
FHD-286. FHD-286 is a potent, first-in-class, selective inhibitor of the SMARCA2 (BRM) and SMARCA4 (BRG1) subunits of the BAF chromatin remodeling complex where dependency on SMARCA2/SMARCA4 is well-established preclinically with multiple tumor types, including acute myeloid leukemia (AML)/myelodysplastic syndrome (MDS), NSCLC and prostate cancer.
- AML Phase 1 trial. The ongoing Phase 1 dose escalation trial is evaluating the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), and preliminary clinical activity of FHD-286 in combination with decitabine or low-dose cytarabine in patients with relapsed and/or refractory AML who have failed multiple courses of therapy. FHD-286 previously demonstrated a promising mutation-agnostic differentiation effect in a single-agent dose escalation trial.
- Topline safety, tolerability, initial efficacy, and PK/PD data expected by year-end 2024.
FHD-909 (LY4050784). FHD-909 is a first-in-class oral SMARCA2 selective inhibitor that has demonstrated in preclinical studies to have high selectivity over its closely related paralog SMARCA4, two proteins that are the catalytic engines across all forms of the BAF complex. SMARCA4 mutations are common across tumor types, including approximately
- Dosed first patient. In October 2024, the first patient was dosed in the Phase 1 trial for FHD-909 in SMARCA4 mutated cancers, with NSCLC as the primary target patient population.
- Strategic collaboration with Lilly. In December 2021, Foghorn announced a strategic collaboration with Lilly to create novel oncology medicines that includes a U.S. 50/50 co-development and co-commercialization agreement for Foghorn’s Selective SMARCA2 oncology program, agreements for a selective inhibitor and a selective degrader, and an additional undisclosed oncology target. The collaboration also includes three discovery programs using Foghorn’s proprietary Gene Traffic Control platform.
Selective CBP degrader program. Foghorn is advancing its Selective CBP degrader program to selectively target CBP in EP300 mutated cancer cells. CBP and EP300 are highly similar acetyltransferases that create a synthetic lethal relationship when EP300 is mutated. Attempts to selectively drug CBP have been challenging due to the high level of similarity between the two proteins, while dual inhibition of CBP/EP300 has been limited by hematopoietic toxicity.
- Robust antitumor activity in EP300 loss tumors. In April, Foghorn presented new pharmacodynamic and pharmacokinetic preclinical data at the 2024 AACR Annual Meeting and during a pipeline update call. In October, Foghorn presented additional data on efficacy, tolerability, and formulation at the 7th Annual TPD & Induced Proximity Summit. These data include:
- Deep and sustained CBP degradation significantly inhibited tumor growth in mouse xenograft solid tumor models.
- Robust monotherapy preclinical anti-tumor activity that was not associated with significant body weight loss, thrombocytopenia or anemia.
- Identification of potent and selective CBP protein degraders with first-in-class potential to address tumors harboring EP300 mutations in many types of cancer, including bladder, gastric and endometrial cancers.
- Identification of long-acting injection formulation that resulted in tumor regression from a single dose in a mouse xenograft efficacy study.
- Investigational New Drug (IND)-enabling studies are on track to initiate by the fourth quarter of 2024.
Selective EP300 degrader program. Foghorn is advancing its Selective EP300 degrader program for CBP mutant and EP300-dependent cancers. Attempts to selectively drug EP300 have been challenging due to the high level of similarity between the two proteins, while dual inhibition of CBP/EP300 has been limited by hematopoietic toxicity.
- Robust anti-tumor activity in CBP mutant and EP300 dependent cancers. In April, Foghorn presented new pharmacodynamic and pharmacokinetic preclinical data at the 2024 AACR Annual Meeting and during a pipeline update call highlighting:
- Well-tolerated in vivo with no observed decrease in platelet levels, with no effects on megakaryocyte viability at pharmacologically relevant concentrations in ex vivo studies.
- Identification of potent and selective EP300 degraders with anti-tumor activity in prostate and hematological malignancies, including prostate cancer, multiple myeloma, and diffuse large B cell lymphoma.
Selective ARID1B degrader program.
ARID1A is the most mutated subunit in the BAF complex and amongst the most mutated proteins in oncology. These mutations lead to a dependency on ARID1B in several types of cancer, including ovarian, endometrial, colorectal, and bladder. Attempts to selectively drug ARID1B have been challenging because of the high degree of similarity between ARID1A and ARID1B and the fact that ARID1B has no enzymatic activity to target.
- Highly potent and selective binders developed. In April, Foghorn presented data demonstrating potent and selective small molecule binders to ARID1B. The Company is in the process of converting these selective binders into heterobifunctional degraders.
Third Quarter 2024 Financial Highlights
- Collaboration Revenues. Collaboration revenue was
$7.8 million for the three months ended September 30, 2024, compared to$17.5 million for the three months ended September 30, 2023. The three months ended September 30, 2023 included$16.1 million revenue from a Merck collaboration that ended in August 2023. The revenue in the three months ended September 30, 2024 was driven by the continued advancement of programs under the Lilly Collaboration Agreement. - Research and Development Expenses. Research and development expenses were
$24.7 million for the three months ended September 30, 2024, compared to$26.3 million for the three months ended September 30, 2023. The decrease is attributed to an increase in Lilly partnered programs of$3.3 million , partially offset by decreases in personnel-related costs, early development and other research external costs and facilities and IT related expenses of$5.0 million .
General and Administrative Expenses. General and administrative expenses were
- Net Loss. Net loss was
$19.1 million for the three months ended September 30, 2024, compared to a net loss of$14.3 million for the three months ended September 30, 2023. - Cash, Cash Equivalents and Marketable Securities. As of September 30, 2024, the Company had
$267.4 million in cash, cash equivalents and marketable securities, providing expected cash runway into 2027.
About FHD-286
FHD-286 is a highly potent, first-in-class, selective, allosteric, and orally available small-molecule, enzymatic inhibitor of SMARCA2 (BRM) and SMARCA4 (BRG1), two highly similar proteins that are the ATPases, or the catalytic engines, of the BAF complex, one of the key regulators within the chromatin regulatory system. In preclinical studies, FHD-286 has shown anti-tumor activity across a broad range of malignancies, including both hematologic and solid tumors.
About AML
Adult acute myeloid leukemia (AML) is a cancer of the blood and bone marrow and the most common type of acute leukemia in adults. AML is a diverse disease associated with multiple genetic mutations. It is diagnosed in about 20,000 people every year in the United States.
About FHD-909
FHD-909 (LY4050784) is a potent, first-in-class, allosteric, and orally available small molecule that selectively inhibits the ATPase activity of SMARCA2 (BRM) over its closely related paralog SMARCA4 (BRG1), two proteins that are the catalytic engines across all forms of the BAF complex, one of the key regulators of the chromatin regulatory system. In preclinical studies, tumors with mutations in SMARCA4 rely on SMARCA2 for their survival. FHD-909 has shown significant anti-tumor activity across multiple SMARCA4 mutant lung tumor models.
About Foghorn Therapeutics
Foghorn® Therapeutics is discovering and developing a novel class of medicines targeting genetically determined dependencies within the chromatin regulatory system. Through its proprietary scalable Gene Traffic Control® platform, Foghorn is systematically studying, identifying, and validating potential drug targets within the chromatin regulatory system. The Company is developing multiple product candidates in oncology. Visit our website at www.foghorntx.com for more information on the Company, and follow us on X (formerly Twitter) and LinkedIn.
Forward-Looking Statements
This press release contains “forward-looking statements.” Forward-looking statements include statements regarding the Company’s clinical trials, including its ongoing Phase 1 trial of FHD-286 in combination with decitabine in relapsed and/or refractory AML patients and the ongoing Phase 1 trial of FHD-909 in SMARCA4-mutated cancers , pre-clinical product candidates, expected timing of clinical data, expected cash runway, expected timing of regulatory filings, and research efforts and other statements identified by words such as “could,” “may,” “might,” “will,” “likely,” “anticipates,” “intends,” “plans,” “seeks,” “believes,” “estimates,” “expects,” “continues,” “projects” and similar references to future periods. Forward-looking statements are based on our current expectations and assumptions regarding capital market conditions, our business, the economy and other future conditions. Because forward-looking statements relate to the future, by their nature, they are subject to inherent uncertainties, risks and changes in circumstances that are difficult to predict. As a result, actual results may differ materially from those contemplated by the forward-looking statements. Important factors that could cause actual results to differ materially from those in the forward-looking statements include regional, national or global political, economic, business, competitive, market and regulatory conditions, including risks relating to our clinical trials and other factors set forth under the heading “Risk Factors” in the Company’s Annual Report on Form 10-K for the year ended December 31, 2023, as filed with the Securities and Exchange Commission. Any forward-looking statement made in this press release speaks only as of the date on which it is made.
Condensed Consolidated Balance Sheets (In thousands) | |||||||
September 30, 2024 | December 31, 2023 | ||||||
Cash, cash equivalents and marketable securities | $ | 267,397 | $ | 234,057 | |||
All other assets | 40,975 | 51,859 | |||||
Total assets | $ | 308,372 | $ | 285,916 | |||
Deferred revenue, total | $ | 282,919 | $ | 302,665 | |||
All other liabilities | 53,740 | 60,441 | |||||
Total liabilities | $ | 336,659 | $ | 363,106 | |||
Total stockholders’ deficit | $ | (28,287 | ) | $ | (77,190 | ) | |
Total liabilities and stockholders’ deficit | $ | 308,372 | $ | 285,916 |
Condensed Consolidated Statements of Operations (In thousands, except share and per share amounts) | |||||||
Three Months Ended September 30, | |||||||
2024 | 2023 | ||||||
Collaboration revenue | $ | 7,808 | $ | 17,478 | |||
Operating expenses: | |||||||
Research and development | 24,689 | 26,251 | |||||
General and administrative | 6,971 | 8,308 | |||||
Total operating expenses | $ | 31,660 | $ | 34,559 | |||
Loss from operations | $ | (23,852 | ) | $ | (17,081 | ) | |
Total other income, net | $ | 4,730 | $ | 3,474 | |||
Provision for income taxes | $ | — | $ | (738 | ) | ||
Net loss | $ | (19,122 | ) | $ | (14,345 | ) | |
Net loss per share attributable to common stockholders—basic and diluted | (0.31 | ) | (0.34 | ) | |||
Weighted average common shares outstanding—basic and diluted | 62,602,848 | 42,025,938 | |||||
Contacts:
Karin Hellsvik, Foghorn Therapeutics Inc. (Investors & Media)
khellsvik@foghorntx.com
Adam Silverstein, ScientPR (Media)
adam@scientpr.com
Peter Kelleher, LifeSci Advisors (Investors)
pkelleher@lifesciadvisors.com
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