Legend Biotech Reports Second Quarter 2024 Results and Recent Highlights
Legend Biotech (NASDAQ: LEGN) reported its Q2 2024 results, highlighting CARVYKTI®'s net trade sales of $186 million. The company received MHRA and Health Canada approvals for CARVYKTI® in earlier treatment lines for multiple myeloma. Positive overall survival results were demonstrated in the CARTITUDE-4 study. Legend Biotech's cash position stood at $1.3 billion as of June 30, 2024, providing runway into 2026.
Financial highlights include license revenue of $90.8 million, up from $15.1 million in Q2 2023, and collaboration revenue of $93.3 million, increased from $58.2 million. The company reported a net loss of $18.2 million, significantly reduced from $199.1 million in the same period last year. Research and development expenses rose to $112.6 million, reflecting ongoing investment in cilta-cel and solid tumor programs.
Legend Biotech (NASDAQ: LEGN) ha riportato i risultati del secondo trimestre 2024, evidenziando le vendite nette di CARVYKTI® pari a 186 milioni di dollari. L'azienda ha ricevuto approvazioni da MHRA e Health Canada per CARVYKTI® in linee di trattamento precedenti per il mieloma multiplo. Sono stati dimostrati positivi risultati di sopravvivenza globale nello studio CARTITUDE-4. La posizione di cassa di Legend Biotech era di 1,3 miliardi di dollari al 30 giugno 2024, garantendo così un margine di operatività fino al 2026.
I punti salienti finanziari includono entrate da licenze di 90,8 milioni di dollari, in aumento rispetto ai 15,1 milioni del secondo trimestre 2023, e entrate da collaborazioni di 93,3 milioni di dollari, incrementate rispetto ai 58,2 milioni. L'azienda ha registrato una perdita netta di 18,2 milioni di dollari, significativamente ridotta rispetto ai 199,1 milioni dello stesso periodo dell'anno scorso. Le spese per ricerca e sviluppo sono aumentate a 112,6 milioni di dollari, riflettendo i continui investimenti nei programmi cilta-cel e nei tumori solidi.
Legend Biotech (NASDAQ: LEGN) anunció sus resultados del segundo trimestre de 2024, destacando ventas netas de CARVYKTI® por 186 millones de dólares. La compañía recibió aprobaciones de MHRA y Health Canada para CARVYKTI® en líneas de tratamiento anteriores para el mieloma múltiple. Se demostraron resultados positivos de supervivencia global en el estudio CARTITUDE-4. La posición de efectivo de Legend Biotech era de 1.3 mil millones de dólares al 30 de junio de 2024, proporcionando un margen operativo hasta 2026.
Los aspectos financieros destacados incluyen ingresos por licencias de 90.8 millones de dólares, un aumento respecto a los 15.1 millones del segundo trimestre de 2023, y ingresos por colaboración de 93.3 millones de dólares, aumentando desde los 58.2 millones. La compañía reportó una pérdida neta de 18.2 millones de dólares, significativamente reducida desde los 199.1 millones en el mismo período del año anterior. Los gastos de investigación y desarrollo aumentaron a 112.6 millones de dólares, reflejando la inversión continua en programas de cilta-cel y tumores sólidos.
레전드 바이오테크 (NASDAQ: LEGN)는 2024년 2분기 실적을 발표하며 CARVYKTI®의 순매출이 1억 8,600만 달러에 달했다고 강조했습니다. 이 회사는 다발성 골수종의 초기 치료 라인에 대한 CARVYKTI®에 대해 MHRA와 캐나다 보건부의 승인을 받았습니다. CARTITUDE-4 연구에서 긍정적인 전체 생존 결과가 입증되었습니다. 2024년 6월 30일 기준으로 레전드 바이오테크의 현금 보유액은 13억 달러로 2026년까지 운영할 여유를 제공합니다.
재무 주요 내용으로는 라이센스 수익이 9,080만 달러로, 2023년 2분기 1,510만 달러에서 증가했으며, 협업 수익이 9,330만 달러로, 5820만 달러에서 증가했습니다. 회사는 순손실이 1,820만 달러라고 보고했으며, 이는 작년 동기 1억 9,910만 달러에서 크게 감소한 수치입니다. 연구 및 개발 비용은 1억 1,260만 달러로 증가하여 cilta-cel 및 고형 종양 프로그램에 대한 지속적인 투자를 반영합니다.
Legend Biotech (NASDAQ: LEGN) a présenté ses résultats du deuxième trimestre 2024, mettant en avant des ventes nettes de CARVYKTI® de 186 millions de dollars. La société a reçu des approbations de la MHRA et de Santé Canada pour CARVYKTI® dans des lignes de traitement antérieures pour le myélome multiple. Des résultats positifs en matière de survie globale ont été démontrés dans l'étude CARTITUDE-4. La position de trésorerie de Legend Biotech s'élevait à 1,3 milliard de dollars au 30 juin 2024, garantissant une marge de manœuvre jusqu'en 2026.
Les points saillants financiers incluent des revenus de licence de 90,8 millions de dollars, en hausse par rapport à 15,1 millions de dollars au deuxième trimestre 2023, et des revenus de collaboration de 93,3 millions de dollars, en augmentation par rapport à 58,2 millions de dollars. La société a annoncé une perte nette de 18,2 millions de dollars, considérablement réduite par rapport à 199,1 millions de dollars au cours de la même période l'année précédente. Les dépenses de recherche et développement ont augmenté à 112,6 millions de dollars, reflétant un investissement continu dans les programmes cilta-cel et les tumeurs solides.
Legend Biotech (NASDAQ: LEGN) hat seine Ergebnisse für das zweite Quartal 2024 veröffentlicht und hebt netto Handelsumsätze von CARVYKTI® in Höhe von 186 Millionen US-Dollar hervor. Das Unternehmen erhielt Genehmigungen von der MHRA und Health Canada für CARVYKTI® in früheren Behandlungszeilen für multiples Myelom. Positive Gesamtergebnisse zur Überlebensrate wurden in der Studie CARTITUDE-4 nachgewiesen. Die Bargeldposition von Legend Biotech belief sich zum 30. Juni 2024 auf 1,3 Milliarden US-Dollar, was einen finanziellen Spielraum bis 2026 bietet.
Finanzielle Höhepunkte umfassen Lizenz Einnahmen von 90,8 Millionen US-Dollar, ein Anstieg von 15,1 Millionen im zweiten Quartal 2023, sowie Kooperationsumsätze von 93,3 Millionen US-Dollar, die von 58,2 Millionen gestiegen sind. Das Unternehmen meldete einen Nettverlust von 18,2 Millionen US-Dollar, der im Vergleich zu 199,1 Millionen im gleichen Zeitraum des Vorjahres erheblich gesenkt wurde. Die Ausgaben für Forschung und Entwicklung stiegen auf 112,6 Millionen US-Dollar, was die fortlaufenden Investitionen in cilta-cel und solide Tumorprogramme widerspiegelt.
- CARVYKTI® net trade sales reached $186 million
- License revenue increased to $90.8 million from $15.1 million year-over-year
- Collaboration revenue grew to $93.3 million from $58.2 million year-over-year
- Net loss reduced significantly to $18.2 million from $199.1 million year-over-year
- Cash position of $1.3 billion, providing runway into 2026
- MHRA and Health Canada approvals for CARVYKTI® in earlier treatment lines
- Positive overall survival results in CARTITUDE-4 study
- Research and development expenses increased to $112.6 million from $95.8 million year-over-year
- Administrative expenses rose to $35.4 million from $27.8 million year-over-year
- Selling and distribution expenses increased to $30.1 million from $21.4 million year-over-year
Insights
Legend Biotech's Q2 2024 results show significant progress. Revenue growth is impressive, with license revenue jumping to
However, expenses are rising across the board, with R&D, administrative and selling costs all increasing. This is expected for a growing biotech company but should be monitored. The cash position of
The regulatory approvals for CARVYKTI® in earlier treatment lines by MHRA and Health Canada are significant milestones. This expansion allows for treating patients with fewer prior therapies, potentially improving outcomes. The positive overall survival results from the CARTITUDE-4 study further validate CARVYKTI®'s efficacy.
The completion of CARTITUDE-5 enrollment and ongoing studies demonstrate a robust clinical development program. The outpatient administration progress is particularly noteworthy, as it could significantly improve patient access and reduce healthcare system burden. However, it's important to monitor long-term safety data as the treatment reaches broader patient populations. The growing momentum in both inpatient and outpatient settings suggests increasing physician confidence in managing this complex therapy.
Legend Biotech's market position is strengthening, evidenced by the growing demand for CARVYKTI®. The expansion into earlier treatment lines opens a larger market opportunity. The
The partnership with Janssen Biotech (Johnson & Johnson) provides valuable commercialization support and milestone payments. The new collaboration with Novartis for LB2102 diversifies the pipeline and could lead to future revenue streams. The planned commercial production at the Obelisc facility in Belgium is important for meeting increasing demand. However, investors should watch for potential competition in the CAR-T space and monitor the company's ability to scale manufacturing to meet demand efficiently.
- CARVYKTI® (ciltacabtagene autoleucel; cilta-cel) net trade sales of approximately
$186 million - MHRA and Health Canada approved CARVYKTI® in earlier lines of treatment for adult patients with relapsed and lenalidomide-refractory multiple myeloma
- CARVYKTI® demonstrates positive overall survival results in second interim analysis of CARTITUDE-4 study
- Cash and cash equivalents, deposits and short-term investments of
$1.3 billion , as of June 30, 2024, which Legend Biotech believes will provide financial runway into 2026, when Legend Biotech anticipates achieving an operating profit
SOMERSET, N.J., Aug. 09, 2024 (GLOBE NEWSWIRE) -- Legend Biotech Corporation (NASDAQ: LEGN) (Legend Biotech), a global leader in cell therapy, today reported its second quarter 2024 unaudited financial results and key corporate highlights.
“In the second quarter, approval of CARVYKTI in the second line increased demand and interest from patients and the healthcare community. Momentum for CARVYTKI is growing and we are excited to see it helping not only later line patients, but an increasing number of earlier line patients. I am encouraged by the progress we have been making in both the inpatient and outpatient settings, enabling more patients to receive our transformative one-time treatment,” said Ying Huang, Ph.D., Chief Executive Officer of Legend Biotech. “We look forward to starting commercial production at our Obelisc facility in Belgium later this year in order to meet the growing demand, and we remain laser-focused on increasing our manufacturing capacity.”
Regulatory Updates
- The United Kingdom’s Medicines and Healthcare products Regulatory Agency (MHRA) approved CARVYKTI® for the treatment of adult patients with relapsed and refractory multiple myeloma, who have received at least one prior therapy, including an immunomodulatory agent (IMiD) and a proteasome inhibitor (PI), have demonstrated disease progression on the last therapy and are refractory to lenalidomide.
- Health Canada approved CARVYKTI® for the treatment of adult patients with multiple myeloma, who have received one to three prior lines of therapy including a PI and an IMiD, and who are refractory to lenalidomide.
Key Business Developments
- Novartis Pharmaceuticals Corporation initiated clinical production in July 2024.
- Completed CARTITUDE 5 enrollment in July 2024.
- Announced positive results from a second interim analysis of the Phase 3 CARTITUDE-4 study demonstrating a statistically significant and clinically meaningful improvement in overall survival for multiple myeloma patients treated with CARVYKTI® versus standard-of-care treatment regimens. These new results will be presented at an upcoming medical meeting and shared with regulatory agencies for label updates worldwide.
- New data from the Phase 2 CARTITUDE-2 Cohort D study and new and updated data from the Phase 3 CARTITUDE-4 study of cilta-cel were featured at the 2024 American Society of Clinical Oncology (ASCO) Annual Meeting (Abstracts #7504 and 7505) and European Hematology Association (EHA) 2024 Hybrid Congress (Abstract #S205).
- On June 28, 2024, Legend Biotech received a milestone payment of
$30 million in connection with the Janssen Agreement. - On August 8, 2024, Peter Salovey, Ph.D., was appointed to the Company's Board of Directors, effective August 9, 2024.
* In December 2017, Legend Biotech entered into an exclusive worldwide collaboration and license agreement with Janssen Biotech, Inc., a Johnson & Johnson company, to develop and commercialize cilta-cel (the Janssen Agreement).
Second Quarter 2024 Financial Results
- License Revenue: License revenue was
$90.8 million for the three months ended June 30, 2024, compared to$15.1 million for the three months ended June 30, 2023. The increase was primarily driven by a$60.0 million increase in revenue that was recognized due to the nature of, and timing of milestones achieved as outlined in the Global Development Plan under the Janssen Agreement for cilta-cel. Additionally, the increase in license revenue is driven by the recognition of$15.7 million of revenue due to the timing of underlying activities performed in connection with the global license agreement with Novartis Pharma AG (the "Novartis License Agreement") to develop, manufacture, and commercialize LB2102 and other potential CAR-T therapies selectively targeting DLL3. Legend Biotech did not recognize any license revenue from the Novartis License Agreement for the three months ended June 30, 2023.
- Collaboration Revenue: Collaboration revenue was
$93.3 million for the three months ended June 30, 2024, compared to$58.2 million for the three months ended June 30, 2023. The increase was primarily due to an increase in revenue generated from sales of CARVYKTI® in connection with the Janssen Agreement.
- Collaboration Cost of Revenue: Collaboration cost of revenue was
$45.4 million for the three months ended June 30, 2024, compared to$32.7 million for the three months ended June 30, 2023. The increase was primarily due to Legend Biotech’s share of the cost of sales in connection with CARVYKTI® sales under the Janssen Agreement.
- Cost of License and Other Revenue: Cost of license and other revenue for the three months ended June 30, 2024, was
$5.1 million and consisted of costs in connection with the Novartis License Agreement. The Company did not incur any cost of license and other revenue for the three months ended June 30, 2023.
- Research and Development Expenses: Research and development expenses were
$112.6 million for the three months ended June 30, 2024, compared to$95.8 million for the three months ended June 30, 2023. The increase was primarily driven by continuous research and development activities in cilta-cel, including start up costs for clinical production in Belgium and continued investment in Legend Biotech’s solid tumor programs.
- Administrative Expenses: Administrative expenses were
$35.4 million for the three months ended June 30, 2024, compared to$27.8 million for the three months ended June 30, 2023. The increase was primarily due to the expansion of administrative functions and infrastructure to increase manufacturing capacity.
- Selling and Distribution Expenses: Selling and distribution expenses were
$30.1 million for the three months ended June 30, 2024, compared to$21.4 million for the three months ended June 30, 2023.The increase was primarily driven by costs associated with commercial activities for cilta-cel, including the expansion of the sales force and second line indication launch preparation.
- Net Loss: Net loss was
$18.2 million for the three months ended June 30, 2024, compared to a net loss of$199.1 million for the three months ended June 30, 2023.
- Cash Position: Cash and cash equivalents, time deposits, and short-term investments were
$1.3 billion as of June 30, 2024.
Webcast/Conference Call Details:
Legend Biotech will host its quarterly earnings call and webcast today at 8:00 a.m. ET. To access the webcast, please visit this weblink.
A replay of the webcast will be available on Legend Biotech’s website at https://investors.legendbiotech.com/events-and-presentations.
About Legend Biotech
Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogeneic chimeric antigen receptor T-cell, gamma-delta T cell and natural killer (NK) cell-based immunotherapy. From our three R&D sites around the world, we apply these innovative technologies to pursue the discovery of cutting-edge therapeutics for patients worldwide.
Learn more at www.legendbiotech.com and follow us on X (formerly Twitter) and LinkedIn.
CAUTIONARY NOTE REGARDING FORWARD-LOOKING STATEMENTS
Statements in this press release about future expectations, plans, and prospects, as well as any other statements regarding matters that are not historical facts, constitute “forward-looking statements” within the meaning of The Private Securities Litigation Reform Act of 1995. These statements include, but are not limited to, statements relating to Legend Biotech’s strategies and objectives; statements relating to CARVYKTI®, including Legend Biotech’s expectations for CARVYKTI® and its therapeutic potential; statements relating to the potential approval of CARVYKTI® for earlier lines of therapy; statements related to Legend Biotech manufacturing expectations for CARVYKTI®; statements related to Legend Biotech’s ability to achieve operating profit; and the potential benefits of Legend Biotech’s product candidates. The words “anticipate,” “believe,” “continue,” “could,” “estimate,” “expect,” “intend,” “may,” “plan,” “potential,” “predict,” “project,” “should,” “target,” “will,” “would” and similar expressions are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words. Actual results may differ materially from those indicated by such forward-looking statements as a result of various important factors. Legend Biotech’s expectations could be affected by, among other things, uncertainties involved in the development of new pharmaceutical products; unexpected clinical trial results, including as a result of additional analysis of existing clinical data or unexpected new clinical data; unexpected regulatory actions or delays, including requests for additional safety and/or efficacy data or analysis of data, or government regulation generally; unexpected delays as a result of actions undertaken, or failures to act, by our third party partners; uncertainties arising from challenges to Legend Biotech’s patent or other proprietary intellectual property protection, including the uncertainties involved in the U.S. litigation process; government, industry, and general product pricing and other political pressures; as well as the other factors discussed in the “Risk Factors” section of Legend Biotech’s Annual Report on Form 20-F filed with the Securities and Exchange Commission on March 19, 2024. Should one or more of these risks or uncertainties materialize, or should underlying assumptions prove incorrect, actual results may vary materially from those described in this press release as anticipated, believed, estimated or expected. Any forward-looking statements contained in this press release speak only as of the date of this press release. Legend Biotech specifically disclaims any obligation to update any forward-looking statement, whether as a result of new information, future events or otherwise.
INVESTOR CONTACT:
Jessie Yeung
Tel: (732) 956-8271
jessie.yeung@legendbiotech.com
PRESS CONTACT:
Mary Ann Ondish
Tel: (914) 552-4625
media@legendbiotech.com
| LEGEND BIOTECH CORPORATION CONDENSED CONSOLIDATED STATEMENTS OF PROFIT OR LOSS | |||||||||||||||
| Three Months Ended June 30, 2024 | Six Months Ended June 30, 2024 | ||||||||||||||
| 2024 | 2023 | 2024 | 2023 | ||||||||||||
| US$’000, except share and per share data | (Unaudited) | (Unaudited) | (Unaudited) | (Unaudited) | |||||||||||
| REVENUE | |||||||||||||||
| License revenue | 90,846 | 15,115 | 103,027 | 15,115 | |||||||||||
| Collaboration revenue | 93,254 | 58,152 | 171,735 | 94,432 | |||||||||||
| Other revenue | 2,423 | 63 | 5,752 | 119 | |||||||||||
| Total revenue | 186,523 | 73,330 | 280,514 | 109,666 | |||||||||||
| Collaboration cost of revenue | (45,355 | ) | (32,672 | ) | (94,456 | ) | (68,285 | ) | |||||||
| Cost of license and other revenue | (5,096 | ) | — | (10,734 | ) | — | |||||||||
| Other income and gains | 29,484 | 16,433 | 93,037 | 20,994 | |||||||||||
| Research and development expenses | (112,626 | ) | (95,791 | ) | (213,590 | ) | (180,680 | ) | |||||||
| Administrative expenses | (35,353 | ) | (27,753 | ) | (67,282 | ) | (49,958 | ) | |||||||
| Selling and distribution expenses | (30,063 | ) | (21,429 | ) | (54,286 | ) | (39,383 | ) | |||||||
| Other expenses | — | (21 | ) | (2 | ) | (7,117 | ) | ||||||||
| Fair value loss of warrant liability | — | (105,750 | ) | — | (85,750 | ) | |||||||||
| Finance costs | (5,484 | ) | (5,185 | ) | (10,959 | ) | (10,298 | ) | |||||||
| LOSS BEFORE TAX | (17,970 | ) | (198,838 | ) | (77,758 | ) | (310,811 | ) | |||||||
| Income tax expense | (226 | ) | (290 | ) | (231 | ) | (418 | ) | |||||||
| LOSS FOR THE PERIOD | (18,196 | ) | (199,128 | ) | (77,989 | ) | (311,229 | ) | |||||||
| Attributable to: | |||||||||||||||
| Ordinary equity holders of the parent | (18,196 | ) | (199,128 | ) | (77,989 | ) | (311,229 | ) | |||||||
| LOSS PER SHARE ATTRIBUTABLE TO ORDINARY EQUITY HOLDERS OF THE PARENT | |||||||||||||||
| Basic | (0.05 | ) | (0.57 | ) | (0.21 | ) | (0.91 | ) | |||||||
| Diluted | (0.05 | ) | (0.57 | ) | (0.21 | ) | (0.91 | ) | |||||||
| ORDINARY SHARES USED IN LOSS PER SHARE COMPUTATION | |||||||||||||||
| Basic | 365,204,154 | 350,517,429 | 364,610,589 | 340,779,779 | |||||||||||
| Diluted | 365,204,154 | 350,517,429 | 364,610,589 | 340,779,779 | |||||||||||
| LEGEND BIOTECH CORPORATION CONDENSED CONSOLIDATED STATEMENTS OF FINANCIAL POSITION | |||||||
| June 30, 2024 | December 31, 2023 | ||||||
| US$’000 | US$’000 | ||||||
| (Unaudited) | |||||||
| NON-CURRENT ASSETS | |||||||
| Property, plant and equipment | 105,018 | 108,725 | |||||
| Advance payments for property, plant and equipment | 295 | 451 | |||||
| Right-of-use assets | 114,718 | 80,502 | |||||
| Time deposits | 4,400 | 4,362 | |||||
| Intangible assets | 2,772 | 4,061 | |||||
| Collaboration prepaid leases | 144,552 | 151,216 | |||||
| Other non-current assets | 1,596 | 1,493 | |||||
| Total non-current assets | 373,351 | 350,810 | |||||
| CURRENT ASSETS | |||||||
| Collaboration inventories | 18,870 | 19,433 | |||||
| Trade receivables | 13,064 | 100,041 | |||||
| Prepayments, other receivables and other assets | 100,628 | 69,251 | |||||
| Financial assets at fair value through profit or loss | 42,201 | 663 | |||||
| Pledged deposits | 431 | 357 | |||||
| Time deposits | 1,048,385 | 30,341 | |||||
| Cash and cash equivalents | 201,253 | 1,277,713 | |||||
| Total current assets | 1,424,832 | 1,497,799 | |||||
| Total assets | 1,798,183 | 1,848,609 | |||||
| CURRENT LIABILITIES | |||||||
| Trade payables | 39,490 | 20,160 | |||||
| Other payables and accruals | 169,531 | 132,802 | |||||
| Government grants | 545 | 68 | |||||
| Lease liabilities | 3,325 | 3,175 | |||||
| Tax payable | 6,566 | 7,203 | |||||
| Contract liabilities | 74,845 | 53,010 | |||||
| Total current liabilities | 294,302 | 216,418 | |||||
| NON-CURRENT LIABILITIES | |||||||
| Collaboration interest-bearing advanced funding | 291,559 | 281,328 | |||||
| Lease liabilities long term | 44,042 | 44,169 | |||||
| Government grants | 6,574 | 7,305 | |||||
| Contract liabilities | 2,704 | 47,962 | |||||
| Other non-current liabilities | — | 56 | |||||
| Total non-current liabilities | 344,879 | 380,820 | |||||
| Total liabilities | 639,181 | 597,238 | |||||
| EQUITY | |||||||
| Share capital | 37 | 36 | |||||
| Reserves | 1,158,965 | 1,251,335 | |||||
| Total ordinary shareholders’ equity | 1,159,002 | 1,251,371 | |||||
| Total equity | 1,159,002 | 1,251,371 | |||||
| Total liabilities and equity | 1,798,183 | 1,848,609 | |||||
| LEGEND BIOTECH CORPORATION CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOW | |||||||||||||||
| Three Months Ended June 30, | Six Months Ended June 30, | ||||||||||||||
| US$’000 | 2024 | 2023 | 2024 | 2023 | |||||||||||
| (Unaudited) | (Unaudited) | (Unaudited) | (Unaudited) | ||||||||||||
| LOSS BEFORE TAX | (17,970 | ) | (198,838 | ) | (77,758 | ) | (310,811 | ) | |||||||
| CASH FLOWS (USED IN)/PROVIDED BY OPERATING ACTIVITIES | (1,651 | ) | (95,730 | ) | 13,867 | (236,783 | ) | ||||||||
| CASH FLOWS USED IN INVESTING ACTIVITIES | (695,631 | ) | (123,581 | ) | (1,091,779 | ) | (105,651 | ) | |||||||
| CASH FLOWS PROVIDED BY FINANCING ACTIVITIES | 955 | 789,890 | 1,786 | 789,604 | |||||||||||
| NET (DECREASE)/INCREASE IN CASH AND CASH EQUIVALENTS | (696,327 | ) | 570,579 | (1,076,126 | ) | 447,170 | |||||||||
| Effect of foreign exchange rate changes, net | 9 | 2,584 | (334 | ) | 12 | ||||||||||
| Cash and cash equivalents at beginning of the period | 897,571 | 660,050 | 1,277,713 | 786,031 | |||||||||||
| CASH AND CASH EQUIVALENTS AT END OF THE PERIOD | 201,253 | 1,233,213 | 201,253 | 1,233,213 | |||||||||||
| ANALYSIS OF BALANCES OF CASH AND CASH EQUIVALENTS | |||||||||||||||
| Cash and bank balances | 1,254,469 | 1,334,482 | 1,254,469 | 1,334,482 | |||||||||||
| Less: Pledged deposits | 431 | 1,246 | 431 | 1,246 | |||||||||||
| Time deposits | 1,052,785 | 100,023 | 1,052,785 | 100,023 | |||||||||||
| Cash and cash equivalents as stated in the statement of financial position | 201,253 | 1,233,213 | 201,253 | 1,233,213 | |||||||||||
| Cash and cash equivalents as stated in the statement of cash flows | 201,253 | 1,233,213 | 201,253 | 1,233,213 | |||||||||||
FAQ
What were CARVYKTI's net trade sales in Q2 2024 for Legend Biotech (LEGN)?
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