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Galecto Reports Third Quarter 2024 Financial Results

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Galecto Inc (NASDAQ: GLTO) reported Q3 2024 financial results and strategic updates. The company completed a strategic review to focus on oncology and liver diseases, acquiring global rights to BRM-1420, a dual ENL-YEATS and FLT3 inhibitor for acute myeloid leukemia (AML). Cash position stood at $19.7 million as of September 30, 2024. Q3 net loss was $3.9 million ($3.39 per share), improved from $8.1 million loss year-over-year. R&D expenses decreased to $1.1 million from $2.6 million, while G&A expenses reduced to $2.7 million from $3.3 million in Q3 2023.

Galecto Inc (NASDAQ: GLTO) ha riportato i risultati finanziari del terzo trimestre 2024 e aggiornamenti strategici. L'azienda ha completato una revisione strategica per concentrarsi sull'oncologia e le malattie epatiche, acquisendo i diritti globali per BRM-1420, un inibitore duale di ENL-YEATS e FLT3 per la leucemia mieloide acuta (LMA). La posizione di liquidità ammontava a $19,7 milioni al 30 settembre 2024. La perdita netta del terzo trimestre è stata di $3,9 milioni ($3,39 per azione), migliorata rispetto a una perdita di $8,1 milioni nello stesso periodo dell'anno precedente. Le spese per ricerca e sviluppo sono scese a $1,1 milioni rispetto ai $2,6 milioni, mentre le spese generali e amministrative sono diminuite a $2,7 milioni dai $3,3 milioni nel terzo trimestre del 2023.

Galecto Inc (NASDAQ: GLTO) informó los resultados financieros del tercer trimestre de 2024 y actualizaciones estratégicas. La empresa completó una revisión estratégica para enfocarse en oncología y enfermedades hepáticas, adquiriendo los derechos globales de BRM-1420, un inhibidor dual de ENL-YEATS y FLT3 para la leucemia mieloide aguda (LMA). La posición de efectivo se situó en $19,7 millones al 30 de septiembre de 2024. La pérdida neta en el tercer trimestre fue de $3,9 millones ($3,39 por acción), mejorando respecto a una pérdida de $8,1 millones en el mismo periodo del año anterior. Los gastos en I+D disminuyeron a $1,1 millones desde $2,6 millones, mientras que los gastos generales y administrativos se redujeron a $2,7 millones desde $3,3 millones en el tercer trimestre de 2023.

Galecto Inc (NASDAQ: GLTO)는 2024년 3분기 재무 결과와 전략적 업데이트를 발표했습니다. 이 회사는 종양학과 간 질환에 집중하기 위해 전략 검토를 완료하고, 급성 골수성 백혈병(AML)을 위한 ENL-YEATS 및 FLT3 이중 억제제인 BRM-1420의 글로벌 권리를 인수했습니다. 2024년 9월 30일 기준 현금 보유액은 $19.7 백만이었습니다. 3분기 순손실은 $3.9 백만 ($3.39 주당)으로, 전년 대비 $8.1 백만의 손실에서 개선되었습니다. 연구개발(R&D) 비용은 $2.6 백만에서 $1.1 백만으로 감소했고, 관리 및 일반(G&A) 비용은 2023년 3분기 $3.3 백만에서 $2.7 백만으로 줄어들었습니다.

Galecto Inc (NASDAQ: GLTO) a annoncé les résultats financiers du troisième trimestre 2024 et des mises à jour stratégiques. L'entreprise a réalisé une révision stratégique pour se concentrer sur l'oncologie et les maladies hépatiques, acquérant les droits mondiaux de BRM-1420, un inhibiteur dual d'ENL-YEATS et de FLT3 pour la leucémie myéloïde aiguë (LMA). La trésorerie s'élevait à 19,7 millions de dollars au 30 septembre 2024. La perte nette du troisième trimestre a été de 3,9 millions de dollars (3,39 dollars par action), en amélioration par rapport à une perte de 8,1 millions de dollars l'année précédente. Les dépenses en R&D ont baissé à 1,1 million de dollars contre 2,6 millions de dollars, tandis que les dépenses administratives et générales ont été réduites à 2,7 millions de dollars, contre 3,3 millions de dollars au troisième trimestre 2023.

Galecto Inc (NASDAQ: GLTO) hat die finanziellen Ergebnisse für das dritte Quartal 2024 und strategische Aktualisierungen veröffentlicht. Das Unternehmen hat eine strategische Überprüfung abgeschlossen, um sich auf Onkologie und Lebererkrankungen zu konzentrieren, und die globalen Rechte an BRM-1420 erworben, einem dualen ENL-YEATS- und FLT3-Inhibitor für akute myeloische Leukämie (AML). Zum 30. September 2024 betrug die Liquiditätsposition 19,7 Millionen US-Dollar. Der Nettoverlust im dritten Quartal lag bei 3,9 Millionen US-Dollar (3,39 US-Dollar pro Aktie) und verbesserte sich im Vergleich zu einem Verlust von 8,1 Millionen US-Dollar im Vorjahr. Die F&E-Ausgaben sanken auf 1,1 Millionen US-Dollar von 2,6 Millionen US-Dollar, während die allgemeinen und administrativen Ausgaben im Vergleich zu 3,3 Millionen US-Dollar im dritten Quartal 2023 auf 2,7 Millionen US-Dollar gesenkt wurden.

Positive
  • Net loss improved to $3.9 million from $8.1 million year-over-year
  • R&D expenses decreased by $1.5 million year-over-year
  • G&A expenses reduced by $0.6 million compared to previous year
  • Cash position of $19.7 million sufficient for at least 12 months of operations
Negative
  • Continued operating losses of $3.9 million in Q3 2024
  • Significant decrease in R&D activities might impact future development pipeline
  • IND submission for BRM-1420 not expected until late 2025/early 2026

Insights

This quarterly report reveals concerning financial metrics for this micro-cap biotech. With a market cap of just $9M and quarterly cash burn of approximately $3.8M, the current cash position of $19.7M provides runway despite management's assertion of 12-month sufficiency. The 58% reduction in R&D expenses to $1.1M from $2.6M YoY signals significant scaling back of research activities, though this helped narrow net losses to $3.9M from $8.1M.

The strategic pivot to oncology and liver diseases, while potentially promising with the BRM-1420 acquisition, comes with execution risks. The timeline for IND submission in late 2025/early 2026 suggests a lengthy path to potential commercialization, raising questions about additional funding needs. The stock's micro-cap status and cash position may necessitate dilutive financing in the future.

The acquisition of BRM-1420, a dual ENL-YEATS and FLT3 inhibitor, represents an interesting strategic move into AML treatment. The compound's reported superior activity compared to existing FLT3 and menin inhibitors in preclinical studies across multiple genotypes is noteworthy. However, the timeline to IND submission is relatively distant and success in preclinical studies doesn't guarantee clinical efficacy.

The ongoing Phase 2 investigator-initiated trial of GB1211 with pembrolizumab in melanoma and head/neck cancer provides near-term clinical catalysts. The combination approach targeting both immune checkpoint and the galectin-3 pathway shows promise, but the significant reduction in R&D spending may impact development timelines and capabilities.

-  Completed strategic review to focus on oncology and severe liver diseases

-  Announced acquisition of global rights to BRM-1420, a dual ENL-YEATS and FLT3 inhibitor for multiple genetic subsets of AML from Bridge Medicines

-  Appointed Dr. Amy Wechsler to the Board of Directors and Matthew Kronmiller as Executive Vice President of Strategy and Chief Business Officer

BOSTON, Nov. 01, 2024 (GLOBE NEWSWIRE) -- Galecto, Inc. (NASDAQ: GLTO), a clinical-stage biotechnology company focused on the development of novel treatments for cancer and severe liver diseases, today reported financial results for the third quarter ended September 30, 2024.

“The third quarter was a pivotal period for Galecto highlighted by the completion of a strategic review to prioritize oncology and liver diseases and subsequent acquisition of BRM-1420, a novel, dual ENL-YEATS, and FLT3 inhibitor for multiple genetic subsets of acute myeloid leukemia (AML) that further strengthens our existing portfolio of first-in-class small molecule agents,” said Dr. Hans Schambye, CEO of Galecto. “As we complete the work required to advance BRM-1420 to clinical trials, our goal is to realize its potential in addressing the needs of underserved AML patient populations. We are also excited about the continued development of GB1211, currently being evaluated in two clinical studies for various oncology indications.”

Corporate Highlights

  • Entered into an Asset Purchase Agreement with Bridge Medicines and acquired global rights to Bridge Medicines’ BRM-1420 program, a novel dual ENL-YEATS and FLT3 inhibitor for multiple genetic subsets of AML. BRM-1420 is a potent and selective inhibitor designed to disrupt key oncogenic pathway signaling. Preclinical data demonstrated BRM-1420’s superior activity to both FLT3 and menin inhibitors in primary AML patient samples across multiple genotypes. Galecto plans to submit an investigational new drug application (IND) for BRM-1420 in the US in late 2025 or early 2026 and initiate clinical studies in patients with AML thereafter.
  • Matthew Kronmiller, Bridge Medicine’s Chief Executive Officer, joined Galecto’s management team as the Executive Vice President of Strategy and Chief Business Officer.
  • Appointed Dr. Amy Wechsler to the Board of Directors. Dr. Wechsler brings extensive biotech leadership experience, successfully guiding companies through critical growth stages.
  • Continued enrollment in the ongoing Phase 2 IIT of GB1211 in combination with pembrolizumab (Keytruda®) in metastatic melanoma and head and neck squamous cell carcinoma.

Third Quarter 2024 Financial Results
Cash, cash equivalents, and investments as of September 30, 2024, were approximately $19.7 million. The Company anticipates that its cash, cash equivalents and investments will be sufficient to fund operating expenses and capital requirements for at least the next twelve months.

Research and development expenses were $1.1 million for the three months ended September 30, 2024, compared to $2.6 million for the three months ended September 30, 2023. The decrease of $1.5 million was due primarily to decreased research and development activities.

General and administrative expenses were $2.7 million for the three months ended September 30, 2024, compared to $3.3 million for the three months ended September 30, 2023. The decrease of $0.6 million was primarily related to decreased personnel related costs.

Net loss attributable to common stockholders for the three months ended September 30, 2024 was $3.9 million or $(3.39) per basic and diluted share, compared with $8.1 million, or $(7.50) per basic and diluted share, for the three months ended September 30, 2023.

About Galecto
Galecto is a clinical-stage biopharmaceutical company committed to realizing the promise of novel treatments for cancer and liver diseases. The Company’s pipeline consists of first-in-class small molecule drug candidates that target cancer and fibrosis signaling pathways, including (i) an orally active galectin-3 inhibitor (GB1211) for the treatment of liver cirrhosis; (ii) an orally active galectin-3 inhibitor (GB1211) in combination with a checkpoint inhibitor for various oncology indications; and (iii) as recently announced, a preclinical dual inhibitor of ENL-YEATS and FLT3 (BRM-1420) for multiple genetic subsets of AML, which Galecto acquired from Bridge Medicines. Galecto intends to use its website as a means of disclosing material non-public information. For regular updates about Galecto, visit www.galecto.com.

Forward-Looking Statements
Certain statements in this press release are forward-looking statements that involve a number of risks and uncertainties. Such forward-looking statements include statements about Galecto’s preclinical and clinical development plans for its product candidates and pipeline, including BRM-1420 and GB1211; BRM-1420's potential to address challenging genetic subsets of AML; and that the Company anticipates that its cash, cash equivalents, and investments will be sufficient to fund operating expenses and capital requirements for at least the next twelve months. The words “may,” “will,” “could,” “would,” “should,” “expect,” “plan,” “anticipate,” “intend,” “believe,” “estimate,” “predict,” “project,” “potential,” “continue,” “target” and similar expressions are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words. For such statements, Galecto claims the protection of the Private Securities Litigation Reform Act of 1995. Actual events or results may differ materially from Galecto’s expectations. Factors that could cause actual results to differ materially from the forward-looking statements include risks and uncertainties related to the development of Galecto’s product candidates and their therapeutic potential, Galecto’s use of funds and whether Galecto's cash resources will be sufficient to fund its continuing operations for the periods and/or trials anticipated, and those disclosed in Galecto’s filings with the Securities and Exchange Commission (SEC), including, but not limited to, Galecto’s Annual Report on Form 10-K, as filed with the SEC on March 8, 2024 and Galecto Quarterly Report on Form 10-Q, as filed with the SEC on November 1, 2024. These forward-looking statements represent Galecto’s judgment as of the time of this release. Galecto disclaims any intent or obligation to update these forward-looking statements, other than as may be required under applicable law.

For more information, contact:

Investors/USMedia/EU
Ashley R. Robinson
arr@lifesciadvisors.com
Sandya von der Weid
svonderweid@lifesciadvisors.com
+1 617 430 7577+41 78 680 0538


GALECTO, INC.

Condensed Consolidated Balance Sheet

(in thousands, except share and per share amounts)

 September 30, December 31,
 2024 2023
 (unaudited)  
    
Cash and cash equivalents$19,678 $21,465
Marketable securities   11,686
Prepaid expenses and other current assets 1,500  3,623
Operating lease right-of-use assets 32  247
Other assets, noncurrent 2,166  1,206
Total assets$23,376 $38,227
    
Current liabilities$2,441 $5,830
Operating lease liabilities, noncurrent   66
Total liabilities 2,441  5,896
Total stockholders’ equity 20,935  32,331
Total liabilities and stockholders' equity$23,376 $38,227



GALECTO, INC.

Condensed Consolidated Statements of Operations and Comprehensive Loss

(in thousands, except share and per share amounts)

(Unaudited)

 Three Months Ended
September 30,
 Nine Months Ended
September 30,
  2024   2023   2024   2023 
Operating expenses:       
Research and development$1,093  $2,551  $5,390  $21,002 
General and administrative 2,747   3,304   8,800   9,504 
Restructuring costs    2,728   968   2,728 
Total operating expenses 3,840   8,583   15,158   33,234 
Loss from operations (3,840)  (8,583)  (15,158)  (33,234)
Total other income (loss), net (36)  447   509   1,360 
Loss before income tax expense (3,876)  (8,136)  (14,649)  (31,874)
Income tax expense 7   -   49   - 
Net loss$(3,883) $(8,136) $(14,698) $(31,874)
Net loss per common share, basic and diluted$(3.39) $(7.50) $(13.30) $(30.20)
Weighted-average number of shares used in computing net loss per common share, basic and diluted 1,144,978   1,084,191   1,104,849   1,055,580 
Other comprehensive gain, net of tax 468   183   285   290 
Total comprehensive loss$(3,415) $(7,953) $(14,413) $(31,584)
        

FAQ

What was Galecto's (GLTO) net loss in Q3 2024?

Galecto reported a net loss of $3.9 million, or $3.39 per basic and diluted share, in Q3 2024.

How much cash does Galecto (GLTO) have as of September 30, 2024?

Galecto had approximately $19.7 million in cash, cash equivalents, and investments as of September 30, 2024.

What is BRM-1420 and when will Galecto (GLTO) start clinical trials?

BRM-1420 is a dual ENL-YEATS and FLT3 inhibitor for acute myeloid leukemia. Galecto plans to submit an IND in late 2025 or early 2026 before initiating clinical trials.

Galecto, Inc.

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