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Rhea-AI Filing Summary

Vericel (VCEL) delivered solid top-line growth in Q2-25 but remains loss-making year-to-date. Revenue rose 20% YoY to $63.2 m, driven mainly by MACI implants (+21% to $53.5 m) and the ongoing launch of NexoBrid (+52% to $1.2 m). Epicel contributed $8.6 m (+11%). Gross margin expanded to 74% (vs. 69%) as the largely fixed Cambridge manufacturing base leveraged higher volumes.

Operating expenses climbed 14% to $48.6 m, led by SG&A (+19% to $41.9 m) reflecting salesforce expansion, MACI Arthro marketing and Burlington facility depreciation. As a result, Q2 operating loss narrowed to $2.0 m (from $6.0 m) and net loss to $0.6 m, or $(0.01) per share. For 1H-25, revenue increased 11% to $115.8 m but net loss widened to $11.8 m due to higher costs.

Balance sheet remains strong: cash & equivalents $80.5 m, investments $83.7 m, no revolver borrowings, giving ~ $164 m liquidity. Operating cash flow was $14.8 m (vs. $25.7 m prior-year) after $22.3 m capex tied to the new Burlington manufacturing site, which will become the primary MACI/Epicel plant once validated.

Strategic highlights: FDA approvals in 2024 expanded MACI to arthroscopic delivery and NexoBrid to pediatric burns; management sees both as growth catalysts. Management projects liquidity is sufficient for at least 12 months.

Vericel (VCEL) ha registrato una solida crescita dei ricavi nel secondo trimestre 2025, ma rimane in perdita da inizio anno. I ricavi sono aumentati del 20% su base annua, raggiungendo 63,2 milioni di dollari, trainati principalmente dagli impianti MACI (+21% a 53,5 milioni) e dal continuo lancio di NexoBrid (+52% a 1,2 milioni). Epicel ha contribuito con 8,6 milioni (+11%). Il margine lordo è salito al 74% (rispetto al 69%) grazie alla base produttiva di Cambridge, in gran parte a costi fissi, che ha beneficiato dei volumi più elevati.

Le spese operative sono aumentate del 14% a 48,6 milioni, principalmente per SG&A (+19% a 41,9 milioni) dovuto all'espansione della forza vendita, al marketing di MACI Arthro e all'ammortamento dello stabilimento di Burlington. Di conseguenza, la perdita operativa del secondo trimestre si è ridotta a 2,0 milioni (da 6,0 milioni) e la perdita netta a 0,6 milioni di dollari, ovvero (0,01) dollari per azione. Nel primo semestre 2025, i ricavi sono cresciuti dell'11% a 115,8 milioni, ma la perdita netta si è ampliata a 11,8 milioni a causa dei costi più elevati.

La situazione patrimoniale rimane solida: liquidità e equivalenti di cassa pari a 80,5 milioni di dollari, investimenti per 83,7 milioni, nessun prestito revolving, per una liquidità complessiva di circa 164 milioni. Il flusso di cassa operativo è stato di 14,8 milioni (rispetto a 25,7 milioni dell'anno precedente) dopo 22,3 milioni di investimenti legati al nuovo sito produttivo di Burlington, che diventerà lo stabilimento principale per MACI/Epicel una volta validato.

Punti strategici: le approvazioni FDA nel 2024 hanno esteso MACI alla somministrazione artroscopica e NexoBrid alle ustioni pediatriche; la direzione considera entrambi come catalizzatori di crescita. La direzione prevede che la liquidità sia sufficiente per almeno 12 mesi.

Vericel (VCEL) registró un sólido crecimiento en ingresos en el segundo trimestre de 2025, aunque sigue reportando pérdidas en lo que va del año. Los ingresos aumentaron un 20% interanual hasta 63,2 millones de dólares, impulsados principalmente por los implantes MACI (+21% a 53,5 millones) y el continuo lanzamiento de NexoBrid (+52% a 1,2 millones). Epicel aportó 8,6 millones (+11%). El margen bruto se amplió al 74% (frente al 69%) gracias a la base de producción de Cambridge, en gran parte de costos fijos, que se benefició de mayores volúmenes.

Los gastos operativos aumentaron un 14% a 48,6 millones, liderados por SG&A (+19% a 41,9 millones) debido a la expansión del equipo de ventas, el marketing de MACI Arthro y la depreciación de las instalaciones de Burlington. Como resultado, la pérdida operativa del segundo trimestre se redujo a 2,0 millones (desde 6,0 millones) y la pérdida neta a 0,6 millones de dólares, o (0,01) dólares por acción. En el primer semestre de 2025, los ingresos aumentaron un 11% a 115,8 millones, pero la pérdida neta se amplió a 11,8 millones debido a mayores costos.

El balance sigue siendo sólido: efectivo y equivalentes por 80,5 millones de dólares, inversiones por 83,7 millones, sin préstamos revolventes, lo que proporciona una liquidez total de aproximadamente 164 millones. El flujo de caja operativo fue de 14,8 millones (frente a 25,7 millones del año anterior) tras una inversión de 22,3 millones vinculada a la nueva planta de Burlington, que se convertirá en la principal para MACI/Epicel una vez validada.

Aspectos estratégicos: las aprobaciones de la FDA en 2024 ampliaron MACI a la entrega artroscópica y NexoBrid a quemaduras pediátricas; la dirección ve ambos como catalizadores de crecimiento. La dirección proyecta que la liquidez es suficiente por al menos 12 meses.

Vericel(VCEL)은 2025년 2분기에 견고한 매출 성장을 기록했으나, 연초부터는 여전히 손실 상태를 유지하고 있습니다. 매출은 전년 동기 대비 20% 증가한 6,320만 달러로, 주로 MACI 임플란트(+21% 5,350만 달러)와 NexoBrid의 지속적인 출시(+52% 120만 달러)가 견인했습니다. Epicel은 860만 달러(+11%)를 기여했습니다. 고정비가 큰 케임브리지 생산기지가 높은 물량을 소화하며 매출총이익률은 69%에서 74%로 확대되었습니다.

영업비용은 14% 증가한 4,860만 달러로, 주로 판매관리비(SG&A)가 19% 증가한 4,190만 달러를 차지했으며, 이는 영업 인력 확장, MACI Arthro 마케팅, 벌링턴 시설 감가상각 때문입니다. 결과적으로 2분기 영업손실은 600만 달러에서 200만 달러로 줄었고, 순손실은 60만 달러, 주당 (0.01) 달러로 감소했습니다. 2025년 상반기 매출은 11% 증가한 1억 1,580만 달러였으나, 비용 상승으로 순손실은 1,180만 달러로 확대되었습니다.

재무 상태는 견고합니다: 현금 및 현금성 자산 8,050만 달러, 투자자산 8,370만 달러, 회전 대출 없음으로 약 1억 6,400만 달러의 유동성을 보유하고 있습니다. 영업 현금 흐름은 1,480만 달러(전년 2,570만 달러 대비)로, 신규 벌링턴 제조 시설과 관련된 2,230만 달러의 자본적 지출 이후입니다. 해당 시설은 검증 후 MACI/Epicel의 주요 공장이 될 예정입니다.

전략적 하이라이트: 2024년 FDA 승인으로 MACI가 관절경 투여로 확대되고 NexoBrid가 소아 화상에 적용되었으며, 경영진은 이를 성장 촉매제로 보고 있습니다. 경영진은 최소 12개월 이상의 유동성이 충분할 것으로 전망합니다.

Vericel (VCEL) a affiché une solide croissance du chiffre d'affaires au deuxième trimestre 2025, mais reste déficitaire depuis le début de l'année. Le chiffre d'affaires a augmenté de 20 % en glissement annuel pour atteindre 63,2 millions de dollars, principalement grâce aux implants MACI (+21 % à 53,5 millions) et au lancement continu de NexoBrid (+52 % à 1,2 million). Epicel a contribué pour 8,6 millions (+11 %). La marge brute s'est élargie à 74 % (contre 69 %) grâce à la base de production de Cambridge, principalement à coûts fixes, qui a tiré parti des volumes plus élevés.

Les charges d'exploitation ont augmenté de 14 % pour atteindre 48,6 millions, principalement portées par les SG&A (+19 % à 41,9 millions) reflétant l'expansion de la force de vente, le marketing de MACI Arthro et l'amortissement de l'installation de Burlington. En conséquence, la perte opérationnelle du deuxième trimestre s'est réduite à 2,0 millions (contre 6,0 millions) et la perte nette à 0,6 million de dollars, soit (0,01) dollar par action. Pour le premier semestre 2025, le chiffre d'affaires a augmenté de 11 % à 115,8 millions, mais la perte nette s'est creusée à 11,8 millions en raison des coûts plus élevés.

Le bilan reste solide : trésorerie et équivalents de trésorerie à 80,5 millions de dollars, investissements à 83,7 millions, pas d'emprunts renouvelables, offrant une liquidité d'environ 164 millions. Le flux de trésorerie opérationnel s'est élevé à 14,8 millions (contre 25,7 millions l'année précédente) après des dépenses d'investissement de 22,3 millions liées au nouveau site de fabrication de Burlington, qui deviendra l'usine principale pour MACI/Epicel une fois validée.

Points stratégiques : les approbations de la FDA en 2024 ont étendu MACI à l'administration arthroscopique et NexoBrid aux brûlures pédiatriques ; la direction considère ces deux éléments comme des catalyseurs de croissance. La direction prévoit que la liquidité est suffisante pour au moins 12 mois.

Vericel (VCEL) verzeichnete im zweiten Quartal 2025 ein solides Umsatzwachstum, bleibt jedoch im laufenden Jahr weiterhin verlustreich. Der Umsatz stieg im Jahresvergleich um 20 % auf 63,2 Mio. USD, hauptsächlich getrieben durch MACI-Implantate (+21 % auf 53,5 Mio. USD) und die fortlaufende Markteinführung von NexoBrid (+52 % auf 1,2 Mio. USD). Epicel trug 8,6 Mio. USD (+11 %) bei. Die Bruttomarge erhöhte sich auf 74 % (vorher 69 %), da die weitgehend fixe Produktionsbasis in Cambridge von höheren Stückzahlen profitierte.

Die Betriebsausgaben stiegen um 14 % auf 48,6 Mio. USD, hauptsächlich bedingt durch SG&A (+19 % auf 41,9 Mio. USD) aufgrund der Erweiterung des Vertriebsteams, Marketing für MACI Arthro und Abschreibungen auf die Anlage in Burlington. Infolgedessen verringerte sich der operative Verlust im zweiten Quartal auf 2,0 Mio. USD (von 6,0 Mio.) und der Nettoverlust auf 0,6 Mio. USD bzw. (0,01) USD je Aktie. Für das erste Halbjahr 2025 stiegen die Umsätze um 11 % auf 115,8 Mio. USD, der Nettoverlust weitete sich jedoch auf 11,8 Mio. USD aufgrund gestiegener Kosten aus.

Die Bilanz bleibt stark: Zahlungsmittel und Zahlungsmitteläquivalente in Höhe von 80,5 Mio. USD, Investitionen von 83,7 Mio. USD, keine revolvierenden Kredite, was eine Liquidität von rund 164 Mio. USD ergibt. Der operative Cashflow betrug 14,8 Mio. USD (vorher 25,7 Mio. USD) nach Investitionen von 22,3 Mio. USD im Zusammenhang mit dem neuen Produktionsstandort in Burlington, der nach Validierung die Hauptanlage für MACI/Epicel werden wird.

Strategische Highlights: Die FDA-Zulassungen im Jahr 2024 erweiterten MACI auf arthroskopische Anwendung und NexoBrid auf pädiatrische Verbrennungen; das Management sieht in beiden Wachstumstreiber. Das Management geht davon aus, dass die Liquidität für mindestens 12 Monate ausreicht.

Positive
  • 20.1% YoY revenue growth and 74% gross margin signal strong demand and operating leverage.
  • Net loss narrowed to $0.6 m in Q2, approaching breakeven.
  • Cash & investments of $164 m with zero debt provides financial flexibility.
  • FDA label expansions for MACI (arthroscopic delivery) and NexoBrid (pediatric) open new market segments.
Negative
  • SG&A expenses up 19%, outpacing revenue and pressuring profitability.
  • 1H-25 net loss widened to $11.8 m despite higher sales.
  • Operating cash flow fell 42% YoY as capex and working-capital needs rose.
  • Epicel sales down 26% for six months, indicating demand volatility.

Insights

TL;DR: Revenue up 20%, near breakeven quarter, liquidity ample; cost creep tempers enthusiasm.

Revenue growth outpaced SG&A, showing early scale benefits from MACI Artho and the NexoBrid rollout. Gross margin at 74% validates the high-value model. Cash plus investments cover >1.4× annual sales and no debt removes refinancing risk. However, stock-based comp ($10.1 m in Q2) and Burlington capex inflate cash burn; operating cash flow halved YoY. Sustained profitability will require SG&A moderation or further top-line acceleration. Guidance absent, but trend suggests FY25 could reach breakeven if Q4 seasonality holds.

TL;DR: Label expansions de-risk growth thesis; execution on Epicel and Burlington validation are watch points.

MACI’s arthroscopic indication enlarges the addressable surgeon pool (~7 k vs 5 k) and should boost volume with less invasive procedures. Pediatric approval for NexoBrid doubles potential burn-unit use cases. Yet Epicel’s 26% 1H sales decline flags competitive or demand variability. Burlington facility, once on-line, could lift capacity and COGS efficiency but introduces validation risk and further depreciation. Overall clinical moat intact, but commercial execution across three therapies must tighten to translate innovation into durable profits.

Vericel (VCEL) ha registrato una solida crescita dei ricavi nel secondo trimestre 2025, ma rimane in perdita da inizio anno. I ricavi sono aumentati del 20% su base annua, raggiungendo 63,2 milioni di dollari, trainati principalmente dagli impianti MACI (+21% a 53,5 milioni) e dal continuo lancio di NexoBrid (+52% a 1,2 milioni). Epicel ha contribuito con 8,6 milioni (+11%). Il margine lordo è salito al 74% (rispetto al 69%) grazie alla base produttiva di Cambridge, in gran parte a costi fissi, che ha beneficiato dei volumi più elevati.

Le spese operative sono aumentate del 14% a 48,6 milioni, principalmente per SG&A (+19% a 41,9 milioni) dovuto all'espansione della forza vendita, al marketing di MACI Arthro e all'ammortamento dello stabilimento di Burlington. Di conseguenza, la perdita operativa del secondo trimestre si è ridotta a 2,0 milioni (da 6,0 milioni) e la perdita netta a 0,6 milioni di dollari, ovvero (0,01) dollari per azione. Nel primo semestre 2025, i ricavi sono cresciuti dell'11% a 115,8 milioni, ma la perdita netta si è ampliata a 11,8 milioni a causa dei costi più elevati.

La situazione patrimoniale rimane solida: liquidità e equivalenti di cassa pari a 80,5 milioni di dollari, investimenti per 83,7 milioni, nessun prestito revolving, per una liquidità complessiva di circa 164 milioni. Il flusso di cassa operativo è stato di 14,8 milioni (rispetto a 25,7 milioni dell'anno precedente) dopo 22,3 milioni di investimenti legati al nuovo sito produttivo di Burlington, che diventerà lo stabilimento principale per MACI/Epicel una volta validato.

Punti strategici: le approvazioni FDA nel 2024 hanno esteso MACI alla somministrazione artroscopica e NexoBrid alle ustioni pediatriche; la direzione considera entrambi come catalizzatori di crescita. La direzione prevede che la liquidità sia sufficiente per almeno 12 mesi.

Vericel (VCEL) registró un sólido crecimiento en ingresos en el segundo trimestre de 2025, aunque sigue reportando pérdidas en lo que va del año. Los ingresos aumentaron un 20% interanual hasta 63,2 millones de dólares, impulsados principalmente por los implantes MACI (+21% a 53,5 millones) y el continuo lanzamiento de NexoBrid (+52% a 1,2 millones). Epicel aportó 8,6 millones (+11%). El margen bruto se amplió al 74% (frente al 69%) gracias a la base de producción de Cambridge, en gran parte de costos fijos, que se benefició de mayores volúmenes.

Los gastos operativos aumentaron un 14% a 48,6 millones, liderados por SG&A (+19% a 41,9 millones) debido a la expansión del equipo de ventas, el marketing de MACI Arthro y la depreciación de las instalaciones de Burlington. Como resultado, la pérdida operativa del segundo trimestre se redujo a 2,0 millones (desde 6,0 millones) y la pérdida neta a 0,6 millones de dólares, o (0,01) dólares por acción. En el primer semestre de 2025, los ingresos aumentaron un 11% a 115,8 millones, pero la pérdida neta se amplió a 11,8 millones debido a mayores costos.

El balance sigue siendo sólido: efectivo y equivalentes por 80,5 millones de dólares, inversiones por 83,7 millones, sin préstamos revolventes, lo que proporciona una liquidez total de aproximadamente 164 millones. El flujo de caja operativo fue de 14,8 millones (frente a 25,7 millones del año anterior) tras una inversión de 22,3 millones vinculada a la nueva planta de Burlington, que se convertirá en la principal para MACI/Epicel una vez validada.

Aspectos estratégicos: las aprobaciones de la FDA en 2024 ampliaron MACI a la entrega artroscópica y NexoBrid a quemaduras pediátricas; la dirección ve ambos como catalizadores de crecimiento. La dirección proyecta que la liquidez es suficiente por al menos 12 meses.

Vericel(VCEL)은 2025년 2분기에 견고한 매출 성장을 기록했으나, 연초부터는 여전히 손실 상태를 유지하고 있습니다. 매출은 전년 동기 대비 20% 증가한 6,320만 달러로, 주로 MACI 임플란트(+21% 5,350만 달러)와 NexoBrid의 지속적인 출시(+52% 120만 달러)가 견인했습니다. Epicel은 860만 달러(+11%)를 기여했습니다. 고정비가 큰 케임브리지 생산기지가 높은 물량을 소화하며 매출총이익률은 69%에서 74%로 확대되었습니다.

영업비용은 14% 증가한 4,860만 달러로, 주로 판매관리비(SG&A)가 19% 증가한 4,190만 달러를 차지했으며, 이는 영업 인력 확장, MACI Arthro 마케팅, 벌링턴 시설 감가상각 때문입니다. 결과적으로 2분기 영업손실은 600만 달러에서 200만 달러로 줄었고, 순손실은 60만 달러, 주당 (0.01) 달러로 감소했습니다. 2025년 상반기 매출은 11% 증가한 1억 1,580만 달러였으나, 비용 상승으로 순손실은 1,180만 달러로 확대되었습니다.

재무 상태는 견고합니다: 현금 및 현금성 자산 8,050만 달러, 투자자산 8,370만 달러, 회전 대출 없음으로 약 1억 6,400만 달러의 유동성을 보유하고 있습니다. 영업 현금 흐름은 1,480만 달러(전년 2,570만 달러 대비)로, 신규 벌링턴 제조 시설과 관련된 2,230만 달러의 자본적 지출 이후입니다. 해당 시설은 검증 후 MACI/Epicel의 주요 공장이 될 예정입니다.

전략적 하이라이트: 2024년 FDA 승인으로 MACI가 관절경 투여로 확대되고 NexoBrid가 소아 화상에 적용되었으며, 경영진은 이를 성장 촉매제로 보고 있습니다. 경영진은 최소 12개월 이상의 유동성이 충분할 것으로 전망합니다.

Vericel (VCEL) a affiché une solide croissance du chiffre d'affaires au deuxième trimestre 2025, mais reste déficitaire depuis le début de l'année. Le chiffre d'affaires a augmenté de 20 % en glissement annuel pour atteindre 63,2 millions de dollars, principalement grâce aux implants MACI (+21 % à 53,5 millions) et au lancement continu de NexoBrid (+52 % à 1,2 million). Epicel a contribué pour 8,6 millions (+11 %). La marge brute s'est élargie à 74 % (contre 69 %) grâce à la base de production de Cambridge, principalement à coûts fixes, qui a tiré parti des volumes plus élevés.

Les charges d'exploitation ont augmenté de 14 % pour atteindre 48,6 millions, principalement portées par les SG&A (+19 % à 41,9 millions) reflétant l'expansion de la force de vente, le marketing de MACI Arthro et l'amortissement de l'installation de Burlington. En conséquence, la perte opérationnelle du deuxième trimestre s'est réduite à 2,0 millions (contre 6,0 millions) et la perte nette à 0,6 million de dollars, soit (0,01) dollar par action. Pour le premier semestre 2025, le chiffre d'affaires a augmenté de 11 % à 115,8 millions, mais la perte nette s'est creusée à 11,8 millions en raison des coûts plus élevés.

Le bilan reste solide : trésorerie et équivalents de trésorerie à 80,5 millions de dollars, investissements à 83,7 millions, pas d'emprunts renouvelables, offrant une liquidité d'environ 164 millions. Le flux de trésorerie opérationnel s'est élevé à 14,8 millions (contre 25,7 millions l'année précédente) après des dépenses d'investissement de 22,3 millions liées au nouveau site de fabrication de Burlington, qui deviendra l'usine principale pour MACI/Epicel une fois validée.

Points stratégiques : les approbations de la FDA en 2024 ont étendu MACI à l'administration arthroscopique et NexoBrid aux brûlures pédiatriques ; la direction considère ces deux éléments comme des catalyseurs de croissance. La direction prévoit que la liquidité est suffisante pour au moins 12 mois.

Vericel (VCEL) verzeichnete im zweiten Quartal 2025 ein solides Umsatzwachstum, bleibt jedoch im laufenden Jahr weiterhin verlustreich. Der Umsatz stieg im Jahresvergleich um 20 % auf 63,2 Mio. USD, hauptsächlich getrieben durch MACI-Implantate (+21 % auf 53,5 Mio. USD) und die fortlaufende Markteinführung von NexoBrid (+52 % auf 1,2 Mio. USD). Epicel trug 8,6 Mio. USD (+11 %) bei. Die Bruttomarge erhöhte sich auf 74 % (vorher 69 %), da die weitgehend fixe Produktionsbasis in Cambridge von höheren Stückzahlen profitierte.

Die Betriebsausgaben stiegen um 14 % auf 48,6 Mio. USD, hauptsächlich bedingt durch SG&A (+19 % auf 41,9 Mio. USD) aufgrund der Erweiterung des Vertriebsteams, Marketing für MACI Arthro und Abschreibungen auf die Anlage in Burlington. Infolgedessen verringerte sich der operative Verlust im zweiten Quartal auf 2,0 Mio. USD (von 6,0 Mio.) und der Nettoverlust auf 0,6 Mio. USD bzw. (0,01) USD je Aktie. Für das erste Halbjahr 2025 stiegen die Umsätze um 11 % auf 115,8 Mio. USD, der Nettoverlust weitete sich jedoch auf 11,8 Mio. USD aufgrund gestiegener Kosten aus.

Die Bilanz bleibt stark: Zahlungsmittel und Zahlungsmitteläquivalente in Höhe von 80,5 Mio. USD, Investitionen von 83,7 Mio. USD, keine revolvierenden Kredite, was eine Liquidität von rund 164 Mio. USD ergibt. Der operative Cashflow betrug 14,8 Mio. USD (vorher 25,7 Mio. USD) nach Investitionen von 22,3 Mio. USD im Zusammenhang mit dem neuen Produktionsstandort in Burlington, der nach Validierung die Hauptanlage für MACI/Epicel werden wird.

Strategische Highlights: Die FDA-Zulassungen im Jahr 2024 erweiterten MACI auf arthroskopische Anwendung und NexoBrid auf pädiatrische Verbrennungen; das Management sieht in beiden Wachstumstreiber. Das Management geht davon aus, dass die Liquidität für mindestens 12 Monate ausreicht.

FALSE000176962800017696282025-07-282025-07-28

UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
___________________________________
FORM 8-K
___________________________________
CURRENT REPORT
Pursuant to Section 13 or 15(d)
of the Securities Exchange Act of 1934

Date of Report (date of earliest event reported): July 31, 2025 (July 28, 2025)
___________________________________
CoreWeave, Inc.
(Exact name of registrant as specified in its charter)
___________________________________

Delaware

001-42563

82-3060021
(State or other jurisdiction of
incorporation or organization)
(Commission File Number)(I.R.S. Employer Identification Number)
290 W Mt. Pleasant Ave., Suite 4100
Livingston, NJ
07039
(Address of registrant's principal executive offices)
(Zip Code)
Registrant's telephone number, including area code: (973) 270-9737
___________________________________
Not Applicable
(Former name or former address, if changed since last report)
___________________________________
Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions (see General Instruction A.2. below):

Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)
Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)
Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))
Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))
Securities registered pursuant to Section 12(b) of the Act:
Title of each class
Trading Symbol
Name of each exchange on which registered
Class A Common Stock, $0.000005 par value per shareCRWVThe Nasdaq Stock Market LLC
Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§240.12b-2 of this chapter).



Emerging growth company    
If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act.




Item 1.01 Entry into a Material Definitive Agreement.

On July 28, 2025, CoreWeave Compute Acquisition Co. V, LLC (“CCAC V”), a Delaware limited liability company and a direct subsidiary of CoreWeave, Inc., a Delaware Corporation (the “Parent”) and CoreWeave Compute Acquisition Co. VII, LLC (“CCAC VII” and together with CCAC V, the “Borrowers”), a Delaware limited liability company and an indirect subsidiary of the Parent as borrowers, entered into a credit agreement (the “Credit Agreement”) with MUFG Bank, Ltd., as administrative agent, U.S. Bank Trust Company, National Association as collateral agent, U.S. Bank National Association, as depository bank, Morgan Stanley Asset Funding, Inc. and MUFG Bank, Ltd. as joint lead arrangers and joint bookrunners, Goldman Sachs Bank USA, as joint lead arranger, and the lenders party thereto, providing for a $2.6 billion delayed draw term loan facility (the “DDTL 3.0 Facility”). The DDTL 3.0 Facility was entered into primarily to finance capital expenditures required to perform a customer contract, including the acquisition of GPU servers and related infrastructure.

Availability and Maturity

The DDTL 3.0 Facility provides for delayed draw term loans available in one or more draws until the commitment termination date in July 2026. The maturity date of the DDTL 3.0 Facility is August 21, 2030.

Interest Rate and Fees

Amounts borrowed under the DDTL 3.0 Facility are subject to an interest rate per annum equal to, at our option, either (a) for base rate loans, an applicable margin of 3.00% plus a base rate (subject to a 0.00% floor) determined by reference to the highest of (i) the prime rate, (ii) the federal funds effective rate plus 0.50%, and (iii) daily simple SOFR plus 1.00% or (b) for SOFR loans, 4.00% plus the daily compounded SOFR, as applicable (subject to a 0.00% floor).The DDTL 3.0 Facility provides for payment of, among others, undrawn fees in an amount equal to 0.50% per annum on the average daily undrawn portion of the DDTL 3.0 Facility, which undrawn fees are payable monthly in arrears.

Guarantees and Security

The obligations of CCAC VII (but not CCAC V) under the DDTL 3.0 Facility are unconditionally guaranteed by the Parent pursuant to a parent guarantee and pledge agreement, dated as of July 28, 2025, by and among the Parent, CCAC VII HoldCo LLC, a Delaware limited liability company (“CCAC VII HoldCo”), U.S. Bank Trust Company, National Association, and the lenders party thereto (the “Parent Guarantee and Pledge Agreement”). All obligations under the DDTL 3.0 Facility are secured by substantially all assets of CCAC VII and a pledge of 100% of the equity interests in CCAC VII held by CCAC VII HoldCo.

Covenants

The Borrowers are required to comply with the following financial covenants, among others:

Debt Service Coverage Ratio. Beginning in April 2027, the Borrowers are required to maintain a debt service coverage ratio of at least 1.40x.

Contract Realization Ratio. Beginning on the last day of the first full calendar month after the initial borrowing under the DDTL 3.0 Facility, the Borrowers are required to maintain a contract realization ratio (the ratio of actual amounts billed or received under the customer contract during the most recently ended consecutive three-month period to the projected contracted cash flows for such three-month period) of 0.85x or more as of the last day of each calendar month.

Certain Other Covenants and Events of Default. The DDTL 3.0 Facility contains a number of other customary negative covenants, and the Credit Agreement contains customary events of default, including payment defaults, failure to perform or observe covenants, cross-defaults with certain other indebtedness, a change of control, and certain bankruptcy events. The Credit Agreement also contains events of default related to certain adverse events with respect to certain material contracts.

The foregoing summary of the DDTL 3.0 Facility does not purport to be complete and is qualified in its entirety by reference to the complete terms of the Credit Agreement and the Parent Guarantee and Pledge Agreement, which are filed as Exhibits 10.1 and 10.2 hereto, respectively, and incorporated by reference into this Item 1.01.

Item 2.03 Creation of a Direct Financial Obligation or an Obligation under an Off-Balance Sheet Arrangement of a Registrant

The information described above under Item 1.01 is incorporated into this Item 2.03 by reference.




Item 7.01. Regulation FD Disclosure

On July 31, 2025, the Parent issued a press release announcing the closing of the DDTL 3.0 Facility. A copy of the press release is attached hereto as Exhibit 99.1 and incorporated herein by reference.

The information contained in this Item 7.01 of this Current Report on Form 8-K, including Exhibit 99.1 hereto, shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), or otherwise subject to the liabilities of that section, nor shall it be deemed incorporated by reference in any filing made by the Parent under the Securities Act of 1933, as amended or the Exchange Act, regardless of any general incorporation language in such filings, unless expressly incorporated by specific reference in such filings.

Item 9.01 Financial Statements and Exhibits

(d) Exhibits.

Exhibit No.Description
10.1
Credit Agreement between CoreWeave Compute Acquisition Co. V, LLC, CoreWeave Compute Acquisition Co. VII, LLC, U.S. Bank National Association, as depository bank, MUFG Bank, Ltd., as administrative agent, U.S. Bank Trust Company, National Association as collateral agent, Morgan Stanley Asset Funding, Inc., MUFG Bank, Ltd. and Goldman Sachs Bank USA, as joint lead arrangers, and other lenders party thereto, dated July 28, 2025.


10.2
Parent Guarantee and Pledge Agreement between CoreWeave, Inc., CCAC VII Holdco LLC and U.S. Bank Trust Company, National Association, and the lenders party thereto, dated July 28, 2025.
99.1
Press Release of the Company relating to the DDTL 3.0 Facility, dated July 31, 2025.
104
Cover Page Interactive Data File (embedded within the Inline XBRL document)



SIGNATURE

Pursuant to the requirements of the Securities Exchange Act of 1934, as amended, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.

Date: July 31, 2025

COREWEAVE, INC.
By:
/s/ Michael Intrator
Name:
Michael Intrator
Title:
Chief Executive Officer

FAQ

How much did VCEL’s revenue grow in Q2 2025?

Total revenue rose 20.1% year over year to $63.2 million.

Did Vericel report a profit in the quarter?

No. Net loss was $0.6 million, or $(0.01) per share, but significantly improved from the $4.7 million loss a year earlier.

What is Vericel’s liquidity position?

As of June 30 2025 the company held $80.5 m in cash and $83.7 m in marketable securities with no outstanding revolver debt.

How did MACI perform versus other products?

MACI sales reached $53.5 m (+21%), representing 85% of total revenue, while Epicel contributed $8.6 m and NexoBrid $1.2 m.

What are the key growth catalysts ahead?

MACI Arthro arthroscopic delivery, NexoBrid pediatric expansion, and the upcoming Burlington manufacturing facility are expected to drive volume and margin gains.
CoreWeave, Inc.

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