Traws Pharma Reports Full Year 2024 Results and Business Highlights
Traws Pharma (NASDAQ: TRAW) reported its full year 2024 financial results and business updates. The company's lead product candidate, tivoxavir marboxil (TXM), showed promising results in bird flu treatment through three animal models and Phase 1 data. The company is pursuing potential accelerated approval via FDA's 'Animal Rule'.
Financial highlights include:
- Cash position of $21.3 million as of December 31, 2024
- R&D expenses increased to $12.8 million from $11.4 million in 2023
- G&A expenses rose to $12.3 million from $9.1 million in 2023
- Net loss of $166.5 million ($35.21 per share) compared to $18.9 million in 2023
The company completed a $20 million financing in December 2024 and expects its cash runway to extend into Q1 2026. CEO Werner Cautreels will retire effective March 31, 2025, with Chairman Iain D. Dukes assuming the role of Interim CEO.
Traws Pharma (NASDAQ: TRAW) ha riportato i risultati finanziari e gli aggiornamenti aziendali per l'intero anno 2024. Il candidato principale del prodotto dell'azienda, tivoxavir marboxil (TXM), ha mostrato risultati promettenti nel trattamento dell'influenza aviaria attraverso tre modelli animali e dati di Fase 1. L'azienda sta perseguendo una potenziale approvazione accelerata attraverso la 'Animal Rule' della FDA.
Tra i punti salienti finanziari:
- Posizione di cassa di 21,3 milioni di dollari al 31 dicembre 2024
- Le spese per R&S sono aumentate a 12,8 milioni di dollari rispetto agli 11,4 milioni del 2023
- Le spese generali e amministrative sono salite a 12,3 milioni di dollari rispetto ai 9,1 milioni del 2023
- Perdita netta di 166,5 milioni di dollari (35,21 dollari per azione) rispetto ai 18,9 milioni del 2023
L'azienda ha completato un finanziamento di 20 milioni di dollari a dicembre 2024 e prevede che la sua liquidità si estenda fino al primo trimestre del 2026. Il CEO Werner Cautreels si ritirerà a partire dal 31 marzo 2025, con il presidente Iain D. Dukes che assumerà il ruolo di CEO ad interim.
Traws Pharma (NASDAQ: TRAW) informó sus resultados financieros y actualizaciones comerciales para el año completo 2024. El candidato principal del producto de la empresa, tivoxavir marboxil (TXM), mostró resultados prometedores en el tratamiento de la gripe aviar a través de tres modelos animales y datos de Fase 1. La empresa está persiguiendo una posible aprobación acelerada a través de la 'Animal Rule' de la FDA.
Los aspectos financieros destacados incluyen:
- Posición de efectivo de 21,3 millones de dólares al 31 de diciembre de 2024
- Los gastos de I+D aumentaron a 12,8 millones de dólares desde 11,4 millones en 2023
- Los gastos generales y administrativos aumentaron a 12,3 millones de dólares desde 9,1 millones en 2023
- Pérdida neta de 166,5 millones de dólares (35,21 dólares por acción) en comparación con 18,9 millones en 2023
La empresa completó un financiamiento de 20 millones de dólares en diciembre de 2024 y espera que su liquidez se extienda hasta el primer trimestre de 2026. El CEO Werner Cautreels se retirará a partir del 31 de marzo de 2025, y el presidente Iain D. Dukes asumirá el cargo de CEO interino.
트로스 제약 (NASDAQ: TRAW)은 2024년 전체 연도 재무 결과 및 사업 업데이트를 보고했습니다. 회사의 주요 제품 후보인 티폭사비르 마르복실 (TXM)은 세 가지 동물 모델과 1상 데이터에서 조류 인플루엔자 치료에 대한 유망한 결과를 보였습니다. 회사는 FDA의 '동물 규칙'을 통해 잠재적인 신속 승인을 추구하고 있습니다.
재무 하이라이트에는 다음이 포함됩니다:
- 2024년 12월 31일 기준으로 2130만 달러의 현금 보유
- 연구 및 개발 비용이 2023년의 1140만 달러에서 1280만 달러로 증가
- 일반 및 관리 비용이 2023년의 910만 달러에서 1230만 달러로 증가
- 2023년의 1890만 달러에 비해 1억 6650만 달러 (주당 35.21 달러)의 순손실
회사는 2024년 12월에 2000만 달러의 자금을 확보했으며, 2026년 1분기까지 현금 소진이 지속될 것으로 예상하고 있습니다. CEO인 베르너 카우트릴스는 2025년 3월 31일부로 은퇴하며, 의장인 아이언 D. 듀크스가 임시 CEO 역할을 맡게 됩니다.
Traws Pharma (NASDAQ: TRAW) a annoncé ses résultats financiers et ses mises à jour commerciales pour l'année complète 2024. Le principal candidat produit de l'entreprise, tivoxavir marboxil (TXM), a montré des résultats prometteurs dans le traitement de la grippe aviaire à travers trois modèles animaux et des données de phase 1. L'entreprise cherche à obtenir une approbation accélérée via la 'Animal Rule' de la FDA.
Les points saillants financiers comprennent :
- Position de trésorerie de 21,3 millions de dollars au 31 décembre 2024
- Les dépenses de R&D ont augmenté à 12,8 millions de dollars contre 11,4 millions en 2023
- Les dépenses générales et administratives ont augmenté à 12,3 millions de dollars contre 9,1 millions en 2023
- Perte nette de 166,5 millions de dollars (35,21 dollars par action) par rapport à 18,9 millions en 2023
L'entreprise a complété un financement de 20 millions de dollars en décembre 2024 et s'attend à ce que sa trésorerie s'étende jusqu'au premier trimestre 2026. Le PDG Werner Cautreels prendra sa retraite à compter du 31 mars 2025, et le président Iain D. Dukes assumera le rôle de PDG par intérim.
Traws Pharma (NASDAQ: TRAW) hat seine Finanzzahlen und Unternehmensupdates für das gesamte Jahr 2024 veröffentlicht. Der Hauptproduktkandidat des Unternehmens, tivoxavir marboxil (TXM), zeigte vielversprechende Ergebnisse in der Behandlung von Vogelgrippe durch drei Tiermodelle und Phase-1-Daten. Das Unternehmen strebt eine potenzielle beschleunigte Genehmigung gemäß der 'Animal Rule' der FDA an.
Zu den finanziellen Highlights gehören:
- Liquide Mittel von 21,3 Millionen Dollar zum 31. Dezember 2024
- F&E-Ausgaben stiegen auf 12,8 Millionen Dollar von 11,4 Millionen im Jahr 2023
- Allgemeine und Verwaltungskosten stiegen auf 12,3 Millionen Dollar von 9,1 Millionen im Jahr 2023
- Nettoverlust von 166,5 Millionen Dollar (35,21 Dollar pro Aktie) im Vergleich zu 18,9 Millionen Dollar im Jahr 2023
Das Unternehmen hat im Dezember 2024 eine Finanzierung in Höhe von 20 Millionen Dollar abgeschlossen und erwartet, dass die Liquidität bis ins erste Quartal 2026 reicht. CEO Werner Cautreels wird zum 31. März 2025 in den Ruhestand treten, und der Vorsitzende Iain D. Dukes wird die Rolle des Interims-CEOs übernehmen.
- Successful completion of $20 million financing with new institutional healthcare investors
- Positive preclinical data for tivoxavir marboxil in three flu models
- Successful completion of Phase 1 studies for tivoxavir marboxil
- Cash runway extended into Q1 2026
- Net loss increased significantly to $166.5 million from $18.9 million in 2023
- R&D expenses increased by $1.4 million to $12.8 million
- G&A expenses rose by $3.2 million to $12.3 million
- CEO transition could create temporary leadership uncertainty
Insights
Traws Pharma's FY2024 results reveal a strategic pivot towards respiratory viral threats, notably positioning tivoxavir marboxil (TXM) as their lead candidate for bird flu (H5N1). The data package for TXM appears compelling - demonstrating antiviral activity across three animal models (including non-human primates and ferrets) plus positive Phase 1 pharmacokinetics in humans.
The company's pursuit of the FDA's "Animal Rule" pathway is particularly significant. This regulatory mechanism allows approval based primarily on animal efficacy data when human efficacy trials aren't ethical or feasible. For an emerging threat like H5N1, this could potentially accelerate TXM's path to market without requiring large-scale human trials.
Financially, the
The operational expenses (
Tivoxavir marboxil’s potential as a single dose therapeutic agent for bird flu supported by significant antiviral activity in three well accepted animal models and positive Phase 1 data
Ongoing FDA interaction to align on path forward for tivoxavir marboxil, including potential for accelerated approval utilizing the “Animal Rule”
Cash Runway to support planned operations into Q1 2026
Investor Update call today, March 31, 2025 at 10:00 AM ET
NEWTOWN, Pa., March 31, 2025 (GLOBE NEWSWIRE) -- Traws Pharma, Inc. (NASDAQ: TRAW) (“Traws Pharma”, “Traws” or “the Company”), a clinical-stage biopharmaceutical company developing novel therapies to target critical threats to human health from respiratory viral diseases, today reported financial results for the year ended December 31, 2024 and provided recent business highlights, with updates to the Company’s investigational programs including lead product candidate, tivoxavir marboxil (TXM) in development for bird flu, and ratutrelvir in development for COVID.
“I believe Traws made outstanding progress over the last year. We re-defined our focus – to treat critical threats to human health from respiratory diseases -- with bird flu as our top priority. Ongoing reports of farm infections and mutated viruses continue to raise the concern that bird flu could present a pandemic risk. We declared tivoxavir marboxil (TXM) as our lead program, and presented preclinical data demonstrating TXM’s potent resistance profile, robust antiviral activity in three validated flu models, plus positive pharmacokinetic results from a Phase 1 study in healthy volunteers. These data supported submission of our pre-IND meeting request to discuss a potential accelerated path to approval under the Animal Rule. In addition, our successful financing, completed in December, provided Traws with
“During our upcoming investor call, planned for today, we look forward to providing an overview of the public health risk and treatment landscape for H5N1 bird flu, and reviewing the preclinical and clinical data, and regulatory strategy for tivoxavir marboxil. In addition, we plan to review the ongoing need for improved COVID therapy to reduce the frequency of clinical rebound and the concomitant risk for long COVID, the opportunity for ratutrelvir, and next steps for both programs,” concluded Dr. Cautreels.
Register for the Investor Event here.
Upcoming Milestones and Recent Highlights:
Upcoming Milestones:
- Bird flu: Provide an update on FDA discussions regarding the Animal Rule: Q2 2025
- Bird flu: Finalize formulation and CMC scale up
- Bird flu: Finalize the development plan and move forward on the path to approval
- COVID: Submit a pre-IND meeting request to engage with the FDA to understand long COVID endpoints: Q2 2025
Recent Product Development & Corporate Highlights:
Bird Flu
Traws Pharma Antiviral Bird Flu Program, Tivoxavir Marboxil, Shows Positive Data in Non-human Primates – (March 24, 2025) Traws Pharma, Inc. today announced positive topline results from a study evaluating the use of tivoxavir marboxil (TXM) as a treatment for non-human primates challenged with a non-lethal dose of H5N1 bird flu.
Traws Pharma’s Bird Flu Drug Candidate, Tivoxavir Marboxil, Presented at ICAR – (March 21, 2025) Traws Pharma, Inc. today announced that positive data supporting the potential for tivoxavir marboxil (TXM) as a bird flu treatment was presented yesterday in a poster at the International Society for Antiviral Research (ICAR 2025), being held in Las Vegas, Nevada.
Traws Pharma Reports Positive Results from An Accepted Bird Flu Model for Anti-Viral Candidate, Tivoxavir Marboxil – (March 03, 2025) Traws Pharma, Inc. today announced positive topline results from ferrets infected with H5N1 bird flu, an accepted animal model for human influenza, when treated with tivoxavir marboxil as a single dose.
Traws Pharma Announces Completion of Phase I Studies with Tivoxavir Marboxil, a Single Dose Oral Investigational Drug for the Treatment and Prevention of H5N1 Bird Flu – (January 23, 2025) Traws Pharma, Inc. today announced completion of Phase I clinical studies of its investigational one-dose influenza (flu) therapy, tivoxavir marboxil (tivoxavir), for the treatment or prevention of H5N1 bird flu.
COVID
Traws Pharma’s COVID-19 Candidate, Ratutrelvir, Presented at ICAR – (March 25, 2025) Traws Pharma, Inc. today announced that positive data supporting the potential for ratutrelvir, a main protease inhibitor, as a treatment for COVID-19, were presented at the International Conference for Antiviral Research (ICAR 2025).
Corporate
Traws Pharma Announces Management Updates – (March 28, 2025) Traws Pharma, Inc. today announced the retirement of Werner Cautreels, PhD, Chief Executive Officer (CEO), effective on or about the close of business on March 31, 2025. Iain D. Dukes, D Phil, will assume the role of Interim CEO. In addition to his new responsibilities, Dr. Dukes will continue to serve as Traws’ Chairman.
Financial Results:
Cash, cash equivalents and short-term investments: As of December 31, 2024, the Company had cash, cash equivalents, and short-term investments of approximately
Research and development (R&D) expense for the 12 months ended December 31, 2024, totaled
General and administrative (G&A) expense for the 12 months ended December 31, 2024, totaled
Net loss: The net loss for the 12 months ended December 31, 2024 was
Shares Outstanding: Traws had 5,073,790 shares of common stock outstanding as of March 26, 2025. The shares outstanding reflect the issuance of 3.9 million shares related to the December 31, 2024 financing.
About Tivoxavir Marboxil
Tivoxavir marboxil (TXM) is an investigational oral, small molecule CAP-dependent endonuclease inhibitor designed to be administered as a single-dose for the treatment of bird flu and seasonal influenza. It has demonstrated potent in vitro activity against a range of influenza strains in preclinical studies, including the highly pathogenic avian flu H5N1 (bird flu). Consistent, positive preclinical data from three species indicate that a single dose of TXM demonstrated a therapeutic effect against H5N1 bird flu. Seasonal influenza represents an estimated multi-billion dollar antiviral market opportunity, largely driven by global health organizations, practice guidelines and government tenders1,2, with upside potential from potential pandemic flu outbreaks including H5N1 bird flu. We believe that these data support further development of tivoxavir marboxil as a treatment for bird flu.
About Ratutrelvir
Ratutrelvir is an investigational oral, small molecule Mpro (3CL protease) inhibitor designed to be a broadly acting treatment for COVID-19, to be used without ritonavir. It has demonstrated in vitro activity against a range of COVID-19 strains. Preclinical and Phase 1 studies show that ratutrelvir does not require co-administration with a metabolic inhibitor, such as ritonavir, which could avoid ritonavir-associated drug-drug interactions3, and potentially enable wider patient use. Phase 1 data also show that ratutrelvir’s pharmacokinetic (PK) profile demonstrated maintenance of target blood plasma levels approximately 13 times above the EC50 using the target Phase 2 dosing regimen of 600 mg/day for ten days, which may also reduce the likelihood of clinical rebound and, consequently, reduce the risk for long COVID.4 Industry data indicate that COVID treatment represents a potential multi-billion dollar market opportunity5,6.
Source information:
- Per link
- TRAW data on file
- https://ascpt.onlinelibrary.wiley.com/doi/pdf/10.1002/cpt.2646
- Carly Herbert et al. (2025) Clinical Infectious Diseases. https://doi.org/10.1093/cid/ciae539
- Pfizer.com 10K report 2024, Feb 27, 2025
- Merck & Co 10K, Feb 25 2025
About Traws Pharma, Inc.
Traws Pharma is a clinical stage biopharmaceutical company dedicated to developing novel therapies to target critical threats to human health in respiratory viral diseases. We are advancing novel investigational antiviral agents that have potent activity against difficult to treat or resistant virus strains that threaten human health. Our product candidates are intended to be safe, with simple dosing regimens. We strive to utilize accelerated clinical trial strategies with a commitment to patients who are especially vulnerable.
The Company’s two antiviral programs are investigational oral small molecules targeting bird flu and seasonal influenza, and COVID-19. Tivoxavir marboxil is in development as a single dose treatment for bird flu and seasonal influenza, targeting the influenza cap-dependent endonuclease (CEN). Ratutrelvir is in development as a ritonavir-independent COVID treatment, targeting the Main protease (Mpro or 3CL protease).
For more information, please visit www.trawspharma.com and follow us on LinkedIn.
Forward-Looking Statements
Some of the statements in this release are forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, Section 21E of the Securities Exchange Act of 1934, as amended, and the Private Securities Litigation Reform Act of 1995, and involve risks and uncertainties including statements regarding the Company, its business and product candidates, including the potential opportunity, benefits, effectiveness, safety, and the clinical and regulatory plans for tivoxavir marboxil and ratutrelvir. The Company has attempted to identify forward-looking statements by terminology including “believes”, “estimates”, “anticipates”, “expects”, “plans”, “intends”, “may”, “could”, “might”, “will”, “should”, “preliminary”, “encouraging”, “approximately” or other words that convey uncertainty of future events or outcomes. Although Traws believes that the expectations reflected in such forward-looking statements are reasonable as of the date made, expectations may prove to have been materially different from the results expressed or implied by such forward looking statements. These statements are only predictions and involve known and unknown risks, uncertainties, and other factors, including the success and timing of Traws’ clinical trials, collaborations, market conditions, regulatory requirements and pathways for approval, the extent of the spread and threat of the bird flu, the ongoing need for improved therapy to reduce the frequency of clinical rebound and the concomitant risk for long COVID, and those discussed under the heading “Risk Factors” in Traws’ filings with the U.S. Securities and Exchange Commission (SEC). Any forward-looking statements contained in this release speak only as of its date. Traws undertakes no obligation to update any forward-looking statements contained in this release to reflect events or circumstances occurring after its date or to reflect the occurrence of unanticipated events, except to the extent required by law.
Traws Pharma Contact:
Nora Brennan
Traws Pharma, Inc.
nbrennan@trawspharma.com
www.trawspharma.com
Investor Contact:
Bruce Mackle
LifeSci Advisors, LLC
646-889-1200
bmackle@lifesciadvisors.com
Traws Pharma, Inc. Consolidated Balance Sheets | |||||||
December 31, | |||||||
2024 | 2023 | ||||||
Assets | |||||||
Current assets: | |||||||
Cash and cash equivalents | $ | 21,338,000 | $ | 20,821,000 | |||
Tax incentive and other receivables | 1,765,000 | 18,000 | |||||
Prepaid expenses and other assets | 1,848,000 | 1,821,000 | |||||
Total current assets | 24,951,000 | 22,660,000 | |||||
Property and equipment, net | 10,000 | 22,000 | |||||
Other assets | 1,000 | 1,000 | |||||
Total assets | $ | 24,962,000 | $ | 22,683,000 | |||
Liabilities and stockholders’ (deficit) equity | |||||||
Current liabilities: | |||||||
Accounts payable | $ | 8,186,000 | $ | 5,619,000 | |||
Accrued expenses and other liabilities | 3,121,000 | 3,375,000 | |||||
Deferred revenue | 226,000 | 226,000 | |||||
Total current liabilities | 11,533,000 | 9,220,000 | |||||
Deferred revenue, non-current | 2,565,000 | 2,791,000 | |||||
Warrant liabilities | 42,494,000 | — | |||||
Total liabilities | 56,592,000 | 12,011,000 | |||||
Stockholders’ (deficit) equity: | |||||||
Series C Preferred stock, | — | — | |||||
Common stock, | 36,000 | 9,000 | |||||
Additional paid in capital | 617,530,000 | 493,317,000 | |||||
Accumulated deficit | (649,154,000 | ) | (482,631,000 | ) | |||
Accumulated other comprehensive loss | (42,000 | ) | (23,000 | ) | |||
Total stockholders’ (deficit) equity | (31,630,000 | ) | 10,672,000 | ||||
Total liabilities and stockholders’ (deficit) equity | $ | 24,962,000 | $ | 22,683,000 | |||
Traws Pharma, Inc. Consolidated Statements of Operations | |||||||
Years ended December 31, | |||||||
2024 | 2023 | ||||||
Revenue | $ | 226,000 | $ | 226,000 | |||
Operating expenses: | |||||||
Acquired in-process research and development | 117,464,000 | — | |||||
Research and development | 12,847,000 | 11,430,000 | |||||
General and administrative | 12,289,000 | 9,094,000 | |||||
Total operating expenses | 142,600,000 | 20,524,000 | |||||
Loss from operations | (142,374,000 | ) | (20,298,000 | ) | |||
Series A warrant and pre-funded warrant expense | (24,438,000 | ) | — | ||||
Other income, net | 289,000 | 1,350,000 | |||||
Net loss | $ | (166,523,000 | ) | $ | (18,948,000 | ) | |
Net loss attributable to common stockholders, basic and diluted | $ | (54,674,000 | ) | $ | (22.57 | ) | |
Weighted-average shares of common stock outstanding, basic and diluted | 1,552,685 | 839,554 | |||||
Net loss per share of common stock, basic and diluted | $ | (35.21 | ) | $ | — | ||
Net loss attributable to Series C Preferred stockholders, basic and diluted | $ | (111,849,000 | ) | $ | — | ||
Weighted-average shares of Series C Preferred outstanding, basic and diluted | 7,941 | — | |||||
Net loss per share of Series C Preferred, basic and diluted | $ | (14,085.00 | ) | $ | — | ||
