NewAmsterdam Pharma Provides Corporate Update and Reports Third Quarter Financial Results
NewAmsterdam Pharma (NAMS) reported Q3 2024 financial results and corporate updates. The company expects topline data from the pivotal Phase 3 TANDEM trial in Q4 2024, earlier than planned due to faster enrollment. Cash position strengthened to $422.7 million as of September 30, 2024. Q3 revenue increased to $29.1 million, up from $2.9 million in Q3 2023. R&D expenses decreased to $35.7 million from $43.4 million year-over-year, while SG&A expenses increased to $18.4 million from $9.1 million. Net loss improved to $16.6 million compared to $47.1 million in Q3 2023.
NewAmsterdam Pharma (NAMS) ha riportato i risultati finanziari del terzo trimestre 2024 e aggiornamenti aziendali. La società si aspetta dati di vendita dal trial pivottale di Fase 3 TANDEM nel quarto trimestre 2024, anticipati rispetto ai piani a causa di un arruolamento più rapido. La posizione di cassa si è rafforzata a 422,7 milioni di dollari al 30 settembre 2024. I ricavi del terzo trimestre sono aumentati a 29,1 milioni di dollari, rispetto ai 2,9 milioni di dollari del terzo trimestre 2023. Le spese per R&S sono diminuite a 35,7 milioni di dollari rispetto ai 43,4 milioni di dollari dell'anno precedente, mentre le spese SG&A sono aumentate a 18,4 milioni di dollari rispetto ai 9,1 milioni di dollari. La perdita netta è migliorata a 16,6 milioni di dollari rispetto ai 47,1 milioni di dollari del terzo trimestre 2023.
NewAmsterdam Pharma (NAMS) informó los resultados financieros del tercer trimestre de 2024 y actualizaciones corporativas. La empresa espera datos de ventas del ensayo pivotal de Fase 3 TANDEM en el cuarto trimestre de 2024, anticipándose a lo planeado debido a un reclutamiento más rápido. La posición de efectivo se fortaleció a 422,7 millones de dólares al 30 de septiembre de 2024. Los ingresos del tercer trimestre aumentaron a 29,1 millones de dólares, frente a los 2,9 millones de dólares en el tercer trimestre de 2023. Los gastos de I+D disminuyeron a 35,7 millones de dólares desde 43,4 millones de dólares en el año anterior, mientras que los gastos SG&A aumentaron a 18,4 millones de dólares desde 9,1 millones de dólares. La pérdida neta mejoró a 16,6 millones de dólares en comparación con 47,1 millones de dólares en el tercer trimestre de 2023.
NewAmsterdam Pharma (NAMS)는 2024년 3분기 재무 결과 및 기업 업데이트를 보고했습니다. 회사는 2024년 4분기에 3상 TANDEM 임상 시험의 주요 결과를 예상하며, 이는 빠른 등록으로 인해 계획보다 앞당겨진 것입니다. 2024년 9월 30일 기준, 현금 보유고는 4억 2,270만 달러로 강화되었습니다. 3분기 수익은 2,910만 달러로 증가했으며, 이는 2023년 3분기의 290만 달러에서 증가한 수치입니다. 연구 및 개발 비용은 3억 5700만 달러로 연간 4억 3400만 달러에서 감소했으며, SG&A 비용은 1,840만 달러로 증가하여 910만 달러에서 상승했습니다. 순손실은 1,660만 달러로 개선되어 2023년 3분기의 4,710만 달러와 비교되었습니다.
NewAmsterdam Pharma (NAMS) a annoncé les résultats financiers du troisième trimestre 2024 ainsi que des mises à jour d'entreprise. La société s'attend à des données de vente de l'essai pivot de Phase 3 TANDEM au quatrième trimestre 2024, plus tôt que prévu en raison d'un recrutement plus rapide. La position de trésorerie s'est renforcée à 422,7 millions de dollars au 30 septembre 2024. Les revenus du troisième trimestre ont augmenté à 29,1 millions de dollars, contre 2,9 millions de dollars au troisième trimestre 2023. Les dépenses en R&D ont diminué à 35,7 millions de dollars par rapport à 43,4 millions de dollars d'une année sur l'autre, tandis que les dépenses SG&A ont augmenté à 18,4 millions de dollars, contre 9,1 millions de dollars. La perte nette s'est améliorée à 16,6 millions de dollars par rapport à 47,1 millions de dollars au troisième trimestre 2023.
NewAmsterdam Pharma (NAMS) hat die Finanzergebnisse für das dritte Quartal 2024 sowie Unternehmensupdates veröffentlicht. Das Unternehmen erwartet im vierten Quartal 2024 Verkaufsdaten aus der entscheidenden Phase-3-Studie TANDEM, die aufgrund einer schnelleren Rekrutierung früher als geplant vorliegen werden. Die Liquiditätsposition hat sich zum 30. September 2024 auf 422,7 Millionen Dollar gestärkt. Die Einnahmen im dritten Quartal stiegen auf 29,1 Millionen Dollar, im Vergleich zu 2,9 Millionen Dollar im dritten Quartal 2023. Die F&E-Ausgaben sanken auf 35,7 Millionen Dollar gegenüber 43,4 Millionen Dollar im Vorjahr, während die SG&A-Ausgaben auf 18,4 Millionen Dollar von 9,1 Millionen Dollar anstiegen. Der Nettoverlust verbesserte sich auf 16,6 Millionen Dollar im Vergleich zu 47,1 Millionen Dollar im dritten Quartal 2023.
- Cash position increased to $422.7 million from $340.5 million at end of 2023
- Revenue grew significantly to $29.1 million from $2.9 million YoY
- Net loss improved to $16.6 million from $47.1 million YoY
- R&D expenses decreased by $7.7 million YoY
- Secured composition of matter patent through 2043 in the US
- SG&A expenses increased by $9.3 million YoY due to organizational expansion
- Still operating at a net loss position
Insights
The Q3 results showcase a strong financial position with several key developments.
R&D expenses decreased to
The accelerated enrollment in the TANDEM trial evaluating obicetrapib-ezetimibe fixed-dose combination represents significant operational efficiency in clinical development. The convergence of both TANDEM and BROADWAY trial readouts in Q4 2024 could provide comprehensive data on obicetrapib's efficacy in both monotherapy and combination settings for patients with HeFH and ASCVD.
The extensive Phase 3 program spanning 12,250 patients across four studies demonstrates robust clinical development strategy. The upcoming additional safety and efficacy data from BROOKLYN trial at AHA Scientific Sessions could provide further validation of obicetrapib's potential as a non-statin alternative in the
– Topline data from pivotal Phase 3 TANDEM trial now expected in 4Q 2024 due to faster than expected enrollment –
– On-track to report topline data from pivotal Phase 3 BROADWAY trial in 4Q 2024 –
– Strong balance sheet with
NAARDEN, The Netherlands and MIAMI, Nov. 06, 2024 (GLOBE NEWSWIRE) -- NewAmsterdam Pharma Company N.V. (Nasdaq: NAMS or “NewAmsterdam” or the “Company”), a late-stage, clinical biopharmaceutical company developing oral, non-statin medicines for patients at risk of cardiovascular disease (“CVD”) with elevated low-density lipoprotein cholesterol (“LDL-C”), for whom existing therapies are not sufficiently effective or well-tolerated, today announced financial results for the three and nine months ended September 30, 2024.
“We are pleased to report another strong quarter, which was marked by continued execution across our ongoing Phase 3 clinical trials. We are excited to announce that due to faster than expected enrollment in our pivotal Phase 3 TANDEM trial evaluating a fixed-dose combination (“FDC”) of obicetrapib and ezetimibe, we now expect to release topline data in the fourth quarter of 2024,” said Michael Davidson, M.D., Chief Executive Officer of NewAmsterdam. “Additionally, we remain on track to announce topline data from our Phase 3 BROADWAY study by year end and continue to advance our 9,500-patient PREVAIL cardiovascular outcomes trial.”
“We believe there is a substantial opportunity to address the unmet needs across cardiovascular disease, one of the leading causes of mortality worldwide. With our recently secured composition of matter patent granting exclusivity through 2043 in the United States, cash which we believe is sufficient to fund our pivotal Phase 3 readouts, and an experienced leadership team at the helm, we are well-positioned to drive our mission forward. We remain focused on our clinical execution and, if approved, ultimately commercializing obicetrapib to transform patient care for the millions of people living with hyperlipidemia,” continued Dr. Davidson.
Clinical Development Updates
NewAmsterdam is developing obicetrapib, an oral, low-dose and once-daily cholesteryl ester transfer protein (“CETP”) inhibitor, as the preferred LDL-C lowering therapy to be used in patients at risk of CVD for whom existing therapies are not sufficiently effective or well-tolerated.
- Due to faster than expected patient enrollment in the pivotal Phase 3 TANDEM trial evaluating the obicetrapib and ezetimibe FDC, in patients with heterozygous familial hypercholesterolemia (“HeFH”) and/or atherosclerotic cardiovascular disease (“ASCVD”) or ASCVD risk equivalents, the Company expects to announce topline data in the fourth quarter of 2024.
Upcoming Potential Milestones
NewAmsterdam’s global, pivotal Phase 3 clinical development program consists of four studies in over 12,250 patients, three for obicetrapib monotherapy and one for a FDC of obicetrapib and ezetimibe. NewAmsterdam currently expects to achieve the following upcoming milestones:
- Announce additional safety and efficacy data from the Phase 3 BROOKLYN trial for obicetrapib monotherapy at the upcoming 2024 AHA Scientific Sessions taking place November 16 – 18 in Chicago, Illinois.
- Announce topline data from the Phase 3 BROADWAY trial for obicetrapib monotherapy in the fourth quarter of 2024. BROADWAY is evaluating obicetrapib in adult patients with HeFH and/or established ASCVD, whose LDL-C is not adequately controlled, despite being on maximally tolerated lipid-lowering therapy.
- Announce topline data from the Phase 3 TANDEM trial evaluating a FDC of obicetrapib and ezetimibe in the fourth quarter of 2024.
Third Quarter Financial Results
- Cash Position: As of September 30, 2024, NewAmsterdam recorded cash of
$422.7 million , compared to$340.5 million as of December 31, 2023. The increase in cash is primarily driven by the proceeds of the follow-on offering conducted earlier this year, the achievement of a clinical development milestone and warrant exercises partially offset by cash outflows related to research and development costs as the Company continues development of obicetrapib and increased spending on selling, general and administrative expenses to support the Company’s growing organization. - Revenue: NewAmsterdam recognized
$29.1 million in revenue for the three months ended September 30, 2024, compared to$2.9 million in the same period in 2023. This increase is primarily due to the achievement of a clinical development milestone from Menarini during the current period. - Research and Development (“R&D”) Expenses: R&D expenses were
$35.7 million for the three months ended September 30, 2024, compared to$43.4 million for the same period in 2023. This decrease was primarily due to a decrease in clinical expenses related to clinical trials which are completed or nearing completion. - Selling, General and Administrative (“SG&A”) Expenses: SG&A expenses were
$18.4 million in three months ended September 30, 2024, compared to$9.1 million for the same period in 2023. This increase was primarily due to an increase in personnel costs related to expansion of the team to support the growth of the organization and investments in capabilities to support the Company’s planned commercial launch of obicetrapib, if approved. - Net loss: Net loss for the three months ended September 30, 2024 was
$16.6 million compared to net loss of$47.1 million for the same period in 2023. The individual components of the change are described above.
About Obicetrapib
Obicetrapib is a novel, oral, low-dose CETP inhibitor that NewAmsterdam is developing to overcome the limitations of current LDL-lowering treatments. In each of the Company’s Phase 2 trials, ROSE2, TULIP, ROSE, and OCEAN, as well as the Company’s Phase 3 BROOKLYN trial, evaluating obicetrapib as monotherapy or combination therapy, the Company observed statistically significant LDL-lowering combined with a side effect profile similar to that of placebo. The Company is conducting an additional Phase 3 pivotal trial BROADWAY, to evaluate obicetrapib as a monotherapy used as an adjunct to maximally tolerated lipid-lowering therapies to provide additional LDL-lowering for CVD patients, and TANDEM, to evaluate obicetrapib and ezetimibe as a fixed-dose combination. The Company began enrolling patients in BROADWAY in January 2022 and in TANDEM in March 2024; completing enrollment of BROADWAY in July 2023, and TANDEM in July 2024. The Company also commenced the Phase 3 PREVAIL cardiovascular outcomes trial in March 2022, which is designed to assess the potential of obicetrapib to reduce occurrences of major adverse cardiovascular events, including cardiovascular death, non-fatal myocardial infarction, non-fatal stroke and non-elective coronary revascularization. NewAmsterdam completed enrollment of PREVAIL in April 2024 and randomized over 9,500 patients. Commercialization rights of obicetrapib in Europe, either as a monotherapy or as part of a fixed dose combination with ezetimibe, for cardiovascular diseases have been exclusively granted to the Menarini Group, an Italy-based, leading international pharmaceutical and diagnostics company.
About NewAmsterdam
NewAmsterdam Pharma (Nasdaq: NAMS) is a late-stage biopharmaceutical company whose mission is to improve patient care in populations with metabolic diseases where currently approved therapies have not been adequate or well tolerated. We seek to fill a significant unmet need for a safe, well-tolerated and convenient LDL-lowering therapy. In multiple phase 3 studies, NewAmsterdam is investigating obicetrapib, an oral, low-dose and once-daily CETP inhibitor, alone or as a fixed-dose combination with ezetimibe, as LDL-C lowering therapies to be used as an adjunct to statin therapy for patients at risk of CVD with elevated LDL-C, for whom existing therapies are not sufficiently effective or well tolerated.
Forward-Looking Statements
Certain statements included in this document that are not historical facts are forward-looking statements for purposes of the safe harbor provisions under the United States Private Securities Litigation Reform Act of 1995. Forward-looking statements generally are accompanied by words such as “believe,” “may,” “will,” “estimate,” “continue,” “anticipate,” “intend,” “expect,” “should,” “would,” “plan,” “predict,” “potential,” “seem,” “seek,” “future,” “outlook” and similar expressions that predict or indicate future events or trends or that are not statements of historical matters. These forward-looking statements include, but are not limited to, statements regarding the Company’s intellectual property and its ability to enforce, and sufficiency of, its patents, the Company’s business and strategic plans, the Company’s commercial opportunity, the therapeutic and curative potential of the Company’s product candidate, the Company’s clinical trials and the timing for enrolling patients, the timing and forums for announcing data, the achievement and timing of regulatory approvals, and plans for commercialization. These statements are based on various assumptions, whether or not identified in this document, and on the current expectations of the Company’s management and are not predictions of actual performance. These forward-looking statements are provided for illustrative purposes only and are not intended to serve as and must not be relied on as a guarantee, an assurance, a prediction, or a definitive statement of fact or probability. Actual events and circumstances are difficult or impossible to predict and may differ from assumptions. Many actual events and circumstances are beyond the control of the Company. These forward-looking statements are subject to a number of risks and uncertainties, including changes in domestic and foreign business, market, financial, political, and legal conditions; risks related to the approval of the Company’s product candidate and the timing of expected regulatory and business milestones, including potential commercialization; ability to negotiate definitive contractual arrangements with potential customers; the impact of competitive product candidates; ability to obtain sufficient supply of materials; global economic and political conditions, including the Russia-Ukraine and Israel-Hamas conflict; the effects of competition on the Company’s future business; and those factors described in the Company’s public filings with the Securities Exchange Commission. Additional risks related to the Company’s business include, but are not limited to: uncertainty regarding outcomes of the Company’s ongoing clinical trials, particularly as they relate to regulatory review and potential approval for its product candidate; risks associated with the Company’s efforts to commercialize a product candidate; the Company’s ability to negotiate and enter into definitive agreements on favorable terms, if at all; the impact of competing product candidates on the Company’s business; intellectual property related claims; the Company’s ability to attract and retain qualified personnel; ability to continue to source the raw materials for its product candidate. If any of these risks materialize or the Company’s assumptions prove incorrect, actual results could differ materially from the results implied by these forward-looking statements. There may be additional risks that the Company does not presently know or that the Company currently believes are immaterial that could also cause actual results to differ from those contained in the forward-looking statements. In addition, forward-looking statements reflect the Company’s expectations, plans, or forecasts of future events and views as of the date of this document and are qualified in their entirety by reference to the cautionary statements herein. The Company anticipates that subsequent events and developments may cause the Company’s assessments to change. These forward-looking statements should not be relied upon as representing the Company’s assessment as of any date subsequent to the date of this communication. Accordingly, undue reliance should not be placed upon the forward-looking statements. Neither the Company nor any of its affiliates undertakes any obligation to update these forward-looking statements, except as may be required by law.
Company Contact
Matthew Philippe
P: 1-917-882-7512
matthew.philippe@newamsterdampharma.com
Media Contact
Spectrum Science on behalf of NewAmsterdam
Bryan Blatstein
P: 1-917-714-2609
bblatstein@spectrumscience.com
Investor Contact
Precision AQ on behalf of NewAmsterdam
Austin Murtagh
P: 1-212-698-8696
austin.murtagh@precisionaq.com
Financial Tables
| NewAmsterdam Pharma Company N.V. | |||||
| Condensed Consolidated Balance Sheets | |||||
| (Unaudited) | |||||
| September 30, 2024 | December 31, 2023 | ||||
| (In thousands of USD) | |||||
| Assets | |||||
| Current assets: | |||||
| Cash | 422,729 | 340,450 | |||
| Prepayments and other receivables | 15,145 | 6,341 | |||
| Total current assets | 437,874 | 346,791 | |||
| Property, plant and equipment, net | 231 | 46 | |||
| Operating right of use asset | 493 | 55 | |||
| Intangible assets | 593 | 170 | |||
| Long term prepaid expenses | - | 35 | |||
| Total assets | 439,191 | 347,097 | |||
| Liabilities and Shareholders' Equity | |||||
| Current liabilities: | |||||
| Accounts payable | 7,039 | 16,923 | |||
| Accrued expenses and other current liabilities | 10,580 | 11,398 | |||
| Deferred revenue, current | 4,495 | 8,942 | |||
| Lease liability, current | 240 | 60 | |||
| Derivative warrant liabilities | 18,901 | 12,574 | |||
| Total current liabilities | 41,255 | 49,897 | |||
| Deferred revenue, net of current portion | - | 1,019 | |||
| Lease liability, net of current portion | 266 | - | |||
| Derivative earnout liability | 18,808 | 7,788 | |||
| Total liabilities | 60,329 | 58,704 | |||
| Commitments and contingencies (Note 10) | |||||
| Shareholders' Equity (deficit): | |||||
| Ordinary shares, | 11,435 | 10,173 | |||
| Additional paid-in capital | 829,399 | 590,771 | |||
| Accumulated loss | (466,394 | ) | (316,973 | ) | |
| Accumulated other comprehensive income | 4,422 | 4,422 | |||
| Total shareholders' equity | 378,862 | 288,393 | |||
| Total liabilities and shareholders' equity | 439,191 | 347,097 | |||
| NewAmsterdam Pharma Company N.V. | |||||||||||||||
| Condensed Consolidated Statements of Operations and Comprehensive Income (Loss) | |||||||||||||||
| (Unaudited) | |||||||||||||||
| For the three months ended September 30, | For the nine months ended September 30, | ||||||||||||||
| 2024 | 2023 | 2024 | 2023 | ||||||||||||
| (In thousands of USD, except share and per share amounts) | |||||||||||||||
| Revenue | 29,111 | 2,941 | 32,791 | 13,287 | |||||||||||
| Operating expenses: | |||||||||||||||
| Research and development expenses | 35,702 | 43,371 | 116,511 | 118,132 | |||||||||||
| Selling, general and administrative expenses | 18,412 | 9,128 | 49,340 | 27,048 | |||||||||||
| Total operating expenses | 54,114 | 52,499 | 165,851 | 145,180 | |||||||||||
| Operating loss | (25,003 | ) | (49,558 | ) | (133,060 | ) | (131,893 | ) | |||||||
| Other income (expense): | |||||||||||||||
| Interest income | 4,443 | 3,059 | 12,396 | 8,615 | |||||||||||
| Fair value change – earnout and warrants | (770 | ) | 2,521 | (30,028 | ) | (4,004 | ) | ||||||||
| Foreign exchange gains/(losses) | 4,682 | (3,155 | ) | 1,270 | (160 | ) | |||||||||
| Loss before tax | (16,648 | ) | (47,133 | ) | (149,422 | ) | (127,442 | ) | |||||||
| Income tax expense | (1 | ) | — | (1 | ) | — | |||||||||
| Loss and comprehensive loss for the period | (16,647 | ) | (47,133 | ) | (149,421 | ) | (127,442 | ) | |||||||
| Net loss per ordinary share: | |||||||||||||||
| Basic and diluted net loss per ordinary share | $ | (0.18 | ) | $ | (0.57 | ) | $ | (1.61 | ) | $ | (1.55 | ) | |||
| Basic and diluted weighted average number of ordinary shares outstanding | 94,754,140 | 82,466,584 | 92,666,874 | 82,058,225 | |||||||||||
| NewAmsterdam Pharma Company N.V. | |||||||||||||||||
| Condensed Consolidated Statements of Shareholders' Equity (Deficit) | |||||||||||||||||
| (Unaudited) | |||||||||||||||||
| (In thousands of USD, except share amounts) | Shares | Amount | Additional Paid-In Capital | Accumulated Loss | Cumulative Translation Adjustments | Total Shareholders' Equity | |||||||||||
| Balance at December 31, 2022 | 81,559,780 | 10,055 | 555,625 | (140,036 | ) | 4,422 | 430,066 | ||||||||||
| Exercise of warrants | 208,032 | 27 | 2,671 | — | — | 2,698 | |||||||||||
| Share-based compensation | — | — | 7,663 | — | — | 7,663 | |||||||||||
| Total loss and comprehensive loss for the period | — | — | — | (42,018 | ) | — | (42,018 | ) | |||||||||
| As at March 31, 2023 | 81,767,812 | 10,082 | 565,959 | (182,054 | ) | 4,422 | 398,409 | ||||||||||
| Exercise of warrants | 541,609 | 70 | 7,444 | — | — | 7,514 | |||||||||||
| Exercise of stock options | 14,910 | 2 | 103 | — | — | 105 | |||||||||||
| Share-based compensation | — | — | 5,606 | — | — | 5,606 | |||||||||||
| Total loss and comprehensive loss for the period | — | — | — | (38,291 | ) | — | (38,291 | ) | |||||||||
| As at June 30, 2023 | 82,324,331 | 10,154 | 579,112 | (220,345 | ) | 4,422 | 373,343 | ||||||||||
| Exercise of warrants | 100 | 0 | 1 | — | — | 1 | |||||||||||
| Exercise of stock options | 145,337 | 19 | 166 | — | — | 185 | |||||||||||
| Share-based compensation | — | — | 5,439 | — | — | 5,439 | |||||||||||
| Total loss and comprehensive loss for the period | — | — | — | (47,133 | ) | — | (47,133 | ) | |||||||||
| As at September 30, 2023 | 82,469,768 | 10,173 | 584,718 | (267,478 | ) | 4,422 | 331,835 | ||||||||||
| Balance at December 31, 2023 | 82,469,768 | 10,173 | 590,771 | (316,973 | ) | 4,422 | 288,393 | ||||||||||
| Issuance of Ordinary Shares and Pre-Funded Warrants, net of issuance costs | 5,871,909 | 759 | 189,207 | — | — | 189,966 | |||||||||||
| Exercise of warrants | 926,698 | 121 | 19,674 | — | — | 19,795 | |||||||||||
| Exercise of stock options | 452,461 | 60 | (609 | ) | — | — | (549 | ) | |||||||||
| Share-based compensation | — | — | 7,965 | — | — | 7,965 | |||||||||||
| Total loss and comprehensive loss for the period | — | — | — | (93,767 | ) | — | (93,767 | ) | |||||||||
| As at March 31, 2024 | 89,720,836 | 11,113 | 807,008 | (410,740 | ) | 4,422 | 411,803 | ||||||||||
| Exercise of warrants | 294,521 | 38 | 6,268 | — | — | 6,306 | |||||||||||
| Share-based compensation | — | — | 8,337 | — | — | 8,337 | |||||||||||
| Total loss and comprehensive loss for the period | — | — | — | (39,007 | ) | — | (39,007 | ) | |||||||||
| As at June 30, 2024 | 90,015,357 | 11,151 | 821,613 | (449,747 | ) | 4,422 | 387,439 | ||||||||||
| Exercise of Pre-Funded Warrants | 2,105,248 | 279 | (279 | ) | — | — | — | ||||||||||
| Exercise of stock options | 45,000 | 5 | 53 | — | — | 58 | |||||||||||
| Share-based compensation | — | — | 8,012 | — | — | 8,012 | |||||||||||
| Total loss and comprehensive loss for the period | — | — | — | (16,647 | ) | — | (16,647 | ) | |||||||||
| As at September 30, 2024 | 92,165,605 | 11,435 | 829,399 | (466,394 | ) | 4,422 | 378,862 | ||||||||||
| NewAmsterdam Pharma Company N.V. | |||||
| Condensed Consolidated Statements of Cash Flows | |||||
| (Unaudited) | |||||
| For the nine months ended September 30, | |||||
| 2024 | 2023 | ||||
| (In thousands of USD) | |||||
| Operating activities: | |||||
| Loss for the period | (149,421 | ) | (127,442 | ) | |
| Non-cash adjustments to reconcile loss before tax to net cash flows: | |||||
| Depreciation and amortization | 62 | 36 | |||
| Non-cash rent expense | 8 | 5 | |||
| Fair value change - derivative earnout and warrants | 30,028 | 4,004 | |||
| Foreign exchange (gains)/losses | (1,270 | ) | 160 | ||
| Share-based compensation | 24,204 | 18,566 | |||
| Changes in working capital: | |||||
| Changes in prepayments (current and non-current) and other receivables | (8,769 | ) | 988 | ||
| Changes in accounts payable | (9,751 | ) | (7,824 | ) | |
| Changes in accrued expenses and other current liabilities | (708 | ) | 11,266 | ||
| Changes in deferred revenue | (5,466 | ) | (7,903 | ) | |
| Net cash (used in)/provided by operating activities | (121,083 | ) | (108,144 | ) | |
| Investing activities: | |||||
| Purchase of property, plant and equipment, including internal use software | (669 | ) | (21 | ) | |
| Net cash used in investing activities | (669 | ) | (21 | ) | |
| Financing activities: | |||||
| Proceeds from offering of Ordinary Shares and Pre-Funded Warrants | 190,481 | — | |||
| Transaction costs on issue of Ordinary Shares and Pre-Funded Warrants | (515 | ) | — | ||
| Proceeds from exercise of warrants | 13,421 | 8,622 | |||
| Proceeds from exercise of options | 498 | 290 | |||
| Payment of withholding taxes related to net share settlement of exercised options | (989 | ) | — | ||
| Net cash provided by financing activities | 202,896 | 8,912 | |||
| Net change in cash | 81,144 | (99,253 | ) | ||
| Foreign exchange differences | 1,135 | (168 | ) | ||
| Cash at the beginning of the period | 340,450 | 467,728 | |||
| Cash at the end of the period | 422,729 | 368,307 | |||
| Noncash financing and investing activities | |||||
| Right-of-use assets obtained in exchange for new operating lease liabilities | 562 | — | |||
FAQ
When will NewAmsterdam Pharma (NAMS) release TANDEM trial results?
What was NewAmsterdam Pharma's (NAMS) Q3 2024 revenue?
How much cash does NewAmsterdam Pharma (NAMS) have as of Q3 2024?
What was NewAmsterdam Pharma's (NAMS) net loss in Q3 2024?
