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[6-K] U Power Limited Current Report (Foreign Issuer)

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Form Type
6-K
Rhea-AI Filing Summary

Alvotech’s July 2025 Form 6-K details governance, commercial, regulatory and financing actions since its Q1 report.

  • Governance: Six directors re-elected; veteran executive Linda Jónsdóttir appointed CFO; COO Faysal Kalmoua exits board and management.
  • Commercial: Advanz Pharma partnership broadened to three new biosimilars (milestones up to €160 m) and separate AVT10 (Cimzia) deal; global Keytruda biosimilar co-development with Dr. Reddy’s.
  • M&A: Acquired Swiss packager Ivers-Lee and Xbrane’s Swedish R&D team plus Cimzia candidate for c.SEK 275 m.
  • Pipeline: CHMP positive opinion for AVT06 (Eylea); AVT23 (Xolair) study shows therapeutic equivalence.
  • Manufacturing risk: FDA pre-approval inspection (26 Jun–4 Jul) issued Form 483 citing operational, documentation and quality control deficiencies; detailed response submitted 25 Jul.
  • Financing: Oversubscribed SDR IPO (SEK 39 m) and institutional placement (SEK 750 m) add >3,000 new holders; term-loan amendment folds second tranche, trims margin to SOFR+6.0%, facility now $1.081 bn, cash $152 m.

New capital and partnerships enhance growth prospects, but regulatory remediation is critical for near-term BLA approvals.

Il Form 6-K di Alvotech di luglio 2025 riporta le azioni di governance, commerciali, regolatorie e finanziarie intraprese dal rapporto del primo trimestre.

  • Governance: Sei amministratori rieletti; la veterana Linda Jónsdóttir nominata CFO; il COO Faysal Kalmoua lascia consiglio e gestione.
  • Commerciale: Partnership con Advanz Pharma ampliata a tre nuovi biosimilari (milestone fino a €160 mln) e accordo separato per AVT10 (Cimzia); co-sviluppo globale del biosimilare Keytruda con Dr. Reddy’s.
  • M&A: Acquisiti il confezionatore svizzero Ivers-Lee e il team R&D svedese di Xbrane più il candidato Cimzia per c.SEK 275 mln.
  • Pipeline: Opinione positiva CHMP per AVT06 (Eylea); studio AVT23 (Xolair) dimostra equivalenza terapeutica.
  • Rischio produttivo: Ispezione FDA pre-approvazione (26 giu–4 lug) ha emesso Form 483 con rilievi su operazioni, documentazione e controllo qualità; risposta dettagliata inviata il 25 lug.
  • Finanziamenti: IPO SDR sovrasottoscritta (SEK 39 mln) e collocamento istituzionale (SEK 750 mln) aggiungono oltre 3.000 nuovi azionisti; emendamento prestito a termine accorpa seconda tranche, riduce margine a SOFR+6,0%, linea ora $1,081 mld, liquidità $152 mln.

Nuovi capitali e partnership rafforzano le prospettive di crescita, ma la risoluzione delle criticità regolatorie è fondamentale per le approvazioni BLA a breve termine.

El Formulario 6-K de Alvotech de julio de 2025 detalla las acciones de gobernanza, comerciales, regulatorias y financieras desde su informe del primer trimestre.

  • Gobernanza: Seis directores reelegidos; la veterana ejecutiva Linda Jónsdóttir nombrada CFO; el COO Faysal Kalmoua sale del consejo y la gestión.
  • Comercial: Ampliada la asociación con Advanz Pharma a tres nuevos biosimilares (hitos hasta €160 millones) y acuerdo separado para AVT10 (Cimzia); co-desarrollo global del biosimilar de Keytruda con Dr. Reddy’s.
  • Fusiones y Adquisiciones: Adquirido el envasador suizo Ivers-Lee y el equipo sueco de I+D de Xbrane, además del candidato Cimzia por c.SEK 275 millones.
  • Pipeline: Opinión positiva del CHMP para AVT06 (Eylea); estudio AVT23 (Xolair) demuestra equivalencia terapéutica.
  • Riesgo de fabricación: Inspección previa a la aprobación de la FDA (26 jun–4 jul) emitió Formulario 483 citando deficiencias operativas, documentales y de control de calidad; respuesta detallada enviada el 25 jul.
  • Financiación: Oferta pública inicial SDR sobresuscrita (SEK 39 millones) y colocación institucional (SEK 750 millones) añaden más de 3.000 nuevos accionistas; enmienda del préstamo a plazo consolida la segunda tranche, reduce margen a SOFR+6.0%, facilidad ahora $1.081 mil millones, efectivo $152 millones.

El nuevo capital y las asociaciones mejoran las perspectivas de crecimiento, pero la remediación regulatoria es crítica para las aprobaciones BLA a corto plazo.

Alvotech의 2025년 7월 Form 6-K는 1분기 보고서 이후의 거버넌스, 상업, 규제 및 자금 조달 활동을 상세히 설명합니다.

  • 거버넌스: 6명의 이사 재선임; 베테랑 임원 Linda Jónsdóttir CFO 임명; COO Faysal Kalmoua는 이사회 및 경영진에서 퇴임.
  • 상업: Advanz Pharma와의 파트너십이 3개의 신규 바이오시밀러(마일스톤 최대 €1억 6천만)와 별도의 AVT10(Cimzia) 계약으로 확대; Dr. Reddy’s와 글로벌 Keytruda 바이오시밀러 공동 개발.
  • M&A: 스위스 포장업체 Ivers-Lee와 Xbrane의 스웨덴 연구개발팀 및 Cimzia 후보 물질을 약 c.SEK 2억 7,500만에 인수.
  • 파이프라인: AVT06(Eylea)에 대한 CHMP 긍정적 의견; AVT23(Xolair) 연구에서 치료적 동등성 확인.
  • 제조 리스크: FDA 사전 승인 검사(6월 26일~7월 4일)에서 운영, 문서화 및 품질 관리 결함을 지적하는 Form 483 발행; 7월 25일 상세 답변 제출.
  • 자금 조달: 초과 청약된 SDR IPO(SEK 3,900만) 및 기관 배정(SEK 7억 5천만)으로 3,000명 이상의 신규 주주 확보; 조건부 대출 수정으로 2차 분할 통합, 마진 SOFR+6.0%로 축소, 시설 규모 $10억 8,100만, 현금 $1억 5,200만.

신규 자본 및 파트너십이 성장 전망을 강화하지만, 단기 BLA 승인에는 규제 개선이 필수적입니다.

Le Formulaire 6-K d'Alvotech de juillet 2025 détaille les actions de gouvernance, commerciales, réglementaires et financières depuis son rapport du premier trimestre.

  • Gouvernance : Six administrateurs réélus ; la vétéran Linda Jónsdóttir nommée CFO ; le COO Faysal Kalmoua quitte le conseil et la direction.
  • Commercial : Partenariat avec Advanz Pharma étendu à trois nouveaux biosimilaires (jalons jusqu'à 160 M€) et accord distinct pour AVT10 (Cimzia) ; co-développement mondial du biosimilaire Keytruda avec Dr. Reddy’s.
  • Fusions & acquisitions : Acquisition de l'emballeur suisse Ivers-Lee et de l'équipe R&D suédoise de Xbrane ainsi que du candidat Cimzia pour environ 275 MSEK.
  • Pipeline : Avis positif du CHMP pour AVT06 (Eylea) ; étude AVT23 (Xolair) montrant une équivalence thérapeutique.
  • Risque de fabrication : Inspection FDA avant approbation (26 juin–4 juillet) ayant émis un Formulaire 483 signalant des déficiences opérationnelles, documentaires et de contrôle qualité ; réponse détaillée soumise le 25 juillet.
  • Financement : IPO SDR sursouscrite (39 MSEK) et placement institutionnel (750 MSEK) ajoutant plus de 3 000 nouveaux actionnaires ; amendement du prêt à terme regroupant la deuxième tranche, réduisant la marge à SOFR+6,0 %, facilité portée à 1,081 Md$, trésorerie 152 M$.

Les nouveaux capitaux et partenariats renforcent les perspectives de croissance, mais la remédiation réglementaire est cruciale pour les approbations BLA à court terme.

Der Form 6-K von Alvotech im Juli 2025 beschreibt Governance-, kommerzielle, regulatorische und finanzielle Maßnahmen seit dem Q1-Bericht.

  • Governance: Sechs Direktoren wiedergewählt; erfahrene Managerin Linda Jónsdóttir zur CFO ernannt; COO Faysal Kalmoua verlässt Vorstand und Management.
  • Kommerziell: Partnerschaft mit Advanz Pharma auf drei neue Biosimilars ausgeweitet (Meilensteine bis zu €160 Mio.) und separater AVT10 (Cimzia)-Deal; globale Co-Entwicklung des Keytruda-Biosimilars mit Dr. Reddy’s.
  • M&A: Übernahme des Schweizer Verpackers Ivers-Lee und des schwedischen F&E-Teams von Xbrane sowie Cimzia-Kandidat für ca. SEK 275 Mio.
  • Pipeline: Positives CHMP-Gutachten für AVT06 (Eylea); AVT23 (Xolair)-Studie zeigt therapeutische Äquivalenz.
  • Herstellungsrisiko: FDA-Vorabgenehmigungsinspektion (26. Juni–4. Juli) stellte Form 483 mit Hinweisen zu betrieblichen, dokumentarischen und Qualitätskontrollmängeln aus; detaillierte Antwort am 25. Juli eingereicht.
  • Finanzierung: Überzeichnetes SDR-IPO (SEK 39 Mio.) und institutionelle Platzierung (SEK 750 Mio.) bringen über 3.000 neue Anteilseigner; Laufzeitkreditänderung fasst zweite Tranche zusammen, reduziert Marge auf SOFR+6,0 %, Kreditlinie jetzt $1,081 Mrd., Cash $152 Mio.

Neues Kapital und Partnerschaften stärken die Wachstumsaussichten, aber regulatorische Nachbesserungen sind für kurzfristige BLA-Zulassungen entscheidend.

Positive
  • €160 m milestone expansion of Advanz Pharma partnership covering three new biosimilars
  • Global Keytruda biosimilar collaboration with Dr. Reddy’s broadens high-value oncology pipeline
  • CHMP positive opinion for AVT06 and successful AVT23 efficacy study de-risk European approvals
  • SEK 789 m equity raises were oversubscribed, adding >3,000 shareholders and improving liquidity
  • Term-loan amendment lowers interest by 50 bp and simplifies capital structure, reducing financing costs
Negative
  • FDA Form 483 cites multiple manufacturing and documentation deficiencies that could delay four pending BLAs
  • Executive turnover with COO departure may disrupt operational continuity during critical remediation phase

Insights

TL;DR – Strong deals and financing offset by FDA Form 483 risk; net impact neutral.

Commercial wins with Advanz (€160 m milestones) and Dr. Reddy’s expand the oncology & autoimmune pipeline while Ivers-Lee adds downstream capacity. SEK 789 m of fresh equity plus a 50 bp interest cut strengthen liquidity and reduce cash burn. However, the Form 483 covers multiple quality-system gaps tied to four BLAs; approval timing for AVT02/03/05/06 now depends on FDA classification, creating binary regulatory risk. Overall, strategic momentum is positive but valuation upside is capped until inspection issues are fully resolved.

TL;DR – Form 483 elevates approval risk; remediation plan is submitted but outcome uncertain.

The inspection observations span manufacturing controls, documentation and lab practices—areas often requiring re-inspection. While management claims some issues are historical, FDA follow-up could delay launch-ready assets and trigger additional costs. Positive CHMP feedback on AVT06 underscores EU progress, yet U.S. revenue inflection depends on clearing the Form 483. Investors should monitor FDA’s classification letter (OAI, VAI or NAI) and potential impact on 2025–26 launch schedules.

Il Form 6-K di Alvotech di luglio 2025 riporta le azioni di governance, commerciali, regolatorie e finanziarie intraprese dal rapporto del primo trimestre.

  • Governance: Sei amministratori rieletti; la veterana Linda Jónsdóttir nominata CFO; il COO Faysal Kalmoua lascia consiglio e gestione.
  • Commerciale: Partnership con Advanz Pharma ampliata a tre nuovi biosimilari (milestone fino a €160 mln) e accordo separato per AVT10 (Cimzia); co-sviluppo globale del biosimilare Keytruda con Dr. Reddy’s.
  • M&A: Acquisiti il confezionatore svizzero Ivers-Lee e il team R&D svedese di Xbrane più il candidato Cimzia per c.SEK 275 mln.
  • Pipeline: Opinione positiva CHMP per AVT06 (Eylea); studio AVT23 (Xolair) dimostra equivalenza terapeutica.
  • Rischio produttivo: Ispezione FDA pre-approvazione (26 giu–4 lug) ha emesso Form 483 con rilievi su operazioni, documentazione e controllo qualità; risposta dettagliata inviata il 25 lug.
  • Finanziamenti: IPO SDR sovrasottoscritta (SEK 39 mln) e collocamento istituzionale (SEK 750 mln) aggiungono oltre 3.000 nuovi azionisti; emendamento prestito a termine accorpa seconda tranche, riduce margine a SOFR+6,0%, linea ora $1,081 mld, liquidità $152 mln.

Nuovi capitali e partnership rafforzano le prospettive di crescita, ma la risoluzione delle criticità regolatorie è fondamentale per le approvazioni BLA a breve termine.

El Formulario 6-K de Alvotech de julio de 2025 detalla las acciones de gobernanza, comerciales, regulatorias y financieras desde su informe del primer trimestre.

  • Gobernanza: Seis directores reelegidos; la veterana ejecutiva Linda Jónsdóttir nombrada CFO; el COO Faysal Kalmoua sale del consejo y la gestión.
  • Comercial: Ampliada la asociación con Advanz Pharma a tres nuevos biosimilares (hitos hasta €160 millones) y acuerdo separado para AVT10 (Cimzia); co-desarrollo global del biosimilar de Keytruda con Dr. Reddy’s.
  • Fusiones y Adquisiciones: Adquirido el envasador suizo Ivers-Lee y el equipo sueco de I+D de Xbrane, además del candidato Cimzia por c.SEK 275 millones.
  • Pipeline: Opinión positiva del CHMP para AVT06 (Eylea); estudio AVT23 (Xolair) demuestra equivalencia terapéutica.
  • Riesgo de fabricación: Inspección previa a la aprobación de la FDA (26 jun–4 jul) emitió Formulario 483 citando deficiencias operativas, documentales y de control de calidad; respuesta detallada enviada el 25 jul.
  • Financiación: Oferta pública inicial SDR sobresuscrita (SEK 39 millones) y colocación institucional (SEK 750 millones) añaden más de 3.000 nuevos accionistas; enmienda del préstamo a plazo consolida la segunda tranche, reduce margen a SOFR+6.0%, facilidad ahora $1.081 mil millones, efectivo $152 millones.

El nuevo capital y las asociaciones mejoran las perspectivas de crecimiento, pero la remediación regulatoria es crítica para las aprobaciones BLA a corto plazo.

Alvotech의 2025년 7월 Form 6-K는 1분기 보고서 이후의 거버넌스, 상업, 규제 및 자금 조달 활동을 상세히 설명합니다.

  • 거버넌스: 6명의 이사 재선임; 베테랑 임원 Linda Jónsdóttir CFO 임명; COO Faysal Kalmoua는 이사회 및 경영진에서 퇴임.
  • 상업: Advanz Pharma와의 파트너십이 3개의 신규 바이오시밀러(마일스톤 최대 €1억 6천만)와 별도의 AVT10(Cimzia) 계약으로 확대; Dr. Reddy’s와 글로벌 Keytruda 바이오시밀러 공동 개발.
  • M&A: 스위스 포장업체 Ivers-Lee와 Xbrane의 스웨덴 연구개발팀 및 Cimzia 후보 물질을 약 c.SEK 2억 7,500만에 인수.
  • 파이프라인: AVT06(Eylea)에 대한 CHMP 긍정적 의견; AVT23(Xolair) 연구에서 치료적 동등성 확인.
  • 제조 리스크: FDA 사전 승인 검사(6월 26일~7월 4일)에서 운영, 문서화 및 품질 관리 결함을 지적하는 Form 483 발행; 7월 25일 상세 답변 제출.
  • 자금 조달: 초과 청약된 SDR IPO(SEK 3,900만) 및 기관 배정(SEK 7억 5천만)으로 3,000명 이상의 신규 주주 확보; 조건부 대출 수정으로 2차 분할 통합, 마진 SOFR+6.0%로 축소, 시설 규모 $10억 8,100만, 현금 $1억 5,200만.

신규 자본 및 파트너십이 성장 전망을 강화하지만, 단기 BLA 승인에는 규제 개선이 필수적입니다.

Le Formulaire 6-K d'Alvotech de juillet 2025 détaille les actions de gouvernance, commerciales, réglementaires et financières depuis son rapport du premier trimestre.

  • Gouvernance : Six administrateurs réélus ; la vétéran Linda Jónsdóttir nommée CFO ; le COO Faysal Kalmoua quitte le conseil et la direction.
  • Commercial : Partenariat avec Advanz Pharma étendu à trois nouveaux biosimilaires (jalons jusqu'à 160 M€) et accord distinct pour AVT10 (Cimzia) ; co-développement mondial du biosimilaire Keytruda avec Dr. Reddy’s.
  • Fusions & acquisitions : Acquisition de l'emballeur suisse Ivers-Lee et de l'équipe R&D suédoise de Xbrane ainsi que du candidat Cimzia pour environ 275 MSEK.
  • Pipeline : Avis positif du CHMP pour AVT06 (Eylea) ; étude AVT23 (Xolair) montrant une équivalence thérapeutique.
  • Risque de fabrication : Inspection FDA avant approbation (26 juin–4 juillet) ayant émis un Formulaire 483 signalant des déficiences opérationnelles, documentaires et de contrôle qualité ; réponse détaillée soumise le 25 juillet.
  • Financement : IPO SDR sursouscrite (39 MSEK) et placement institutionnel (750 MSEK) ajoutant plus de 3 000 nouveaux actionnaires ; amendement du prêt à terme regroupant la deuxième tranche, réduisant la marge à SOFR+6,0 %, facilité portée à 1,081 Md$, trésorerie 152 M$.

Les nouveaux capitaux et partenariats renforcent les perspectives de croissance, mais la remédiation réglementaire est cruciale pour les approbations BLA à court terme.

Der Form 6-K von Alvotech im Juli 2025 beschreibt Governance-, kommerzielle, regulatorische und finanzielle Maßnahmen seit dem Q1-Bericht.

  • Governance: Sechs Direktoren wiedergewählt; erfahrene Managerin Linda Jónsdóttir zur CFO ernannt; COO Faysal Kalmoua verlässt Vorstand und Management.
  • Kommerziell: Partnerschaft mit Advanz Pharma auf drei neue Biosimilars ausgeweitet (Meilensteine bis zu €160 Mio.) und separater AVT10 (Cimzia)-Deal; globale Co-Entwicklung des Keytruda-Biosimilars mit Dr. Reddy’s.
  • M&A: Übernahme des Schweizer Verpackers Ivers-Lee und des schwedischen F&E-Teams von Xbrane sowie Cimzia-Kandidat für ca. SEK 275 Mio.
  • Pipeline: Positives CHMP-Gutachten für AVT06 (Eylea); AVT23 (Xolair)-Studie zeigt therapeutische Äquivalenz.
  • Herstellungsrisiko: FDA-Vorabgenehmigungsinspektion (26. Juni–4. Juli) stellte Form 483 mit Hinweisen zu betrieblichen, dokumentarischen und Qualitätskontrollmängeln aus; detaillierte Antwort am 25. Juli eingereicht.
  • Finanzierung: Überzeichnetes SDR-IPO (SEK 39 Mio.) und institutionelle Platzierung (SEK 750 Mio.) bringen über 3.000 neue Anteilseigner; Laufzeitkreditänderung fasst zweite Tranche zusammen, reduziert Marge auf SOFR+6,0 %, Kreditlinie jetzt $1,081 Mrd., Cash $152 Mio.

Neues Kapital und Partnerschaften stärken die Wachstumsaussichten, aber regulatorische Nachbesserungen sind für kurzfristige BLA-Zulassungen entscheidend.

 

 

UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

 

FORM 6-K

 

REPORT OF FOREIGN PRIVATE ISSUER
PURSUANT TO RULE 13a-16 OR 15d-16
UNDER THE SECURITIES EXCHANGE ACT OF 1934

 

For the month of July 2025

 

Commission File Number: 001-41679

 

U Power Limited

(Translation of Registrant’s Name into English)

 

18/F, Building 3, Science and Technology Industrial Park

Yijiang District, Wuhu City, Anhui Province

People’s Republic of China, 241003

(Address of principal executive offices)

 

Indicate by check mark whether the registrant files or will file annual reports under cover Form 20-F or Form 40-F.

 

Form 20-F ☒ Form 40-F ☐

 

 

 

 

 

 

INFORMATION CONTAINED IN THIS FORM 6-K REPORT 

 

On July 24, 2025, U Power Limited (the “Company”) entered into a securities purchase agreement (the “Purchase Agreement”) with a certain institutional investor signatory thereto (the “Purchaser”), pursuant to which the Company agreed to issue and sell, in a registered direct offering (the “Registered Direct Offering”): (i) 445,000 Class A ordinary shares (the “Class A Ordinary Shares”) of the Company, par value $0.00001 per share (the “Shares”); and (ii) pre-funded warrants to purchase up to 106,628 Class A Ordinary Shares (the “Pre-Funded Warrants”). The Purchaser also received unregistered common warrants to purchase up to 551,628 Class A Ordinary Shares (the “Common Warrants”) in a concurrent private placement. The purchase price for each Class A Ordinary Share and accompanying Common Warrant was $2.50 and the purchase price for each Pre-Funded Warrant and accompanying Common Warrant was $2.4999.

 

The Registered Direct Offering and concurrent private placement closed on July 25, 2025. The Company received approximately $1,400,000 in gross proceeds from the Registered Direct Offering and concurrent private placement, before deducting placement agent fees and estimated offering expenses. The Company intends to use the net proceeds from the Registered Direct Offering and concurrent private placement for market expansion efforts and business development, working capital and general corporate purposes.

 

The Pre-Funded Warrants were sold to the Purchaser, whose purchase of the Class A Ordinary Shares in the Registered Direct Offering would otherwise have resulted in such Purchaser, together with its affiliates and certain related parties, beneficially owning more than 4.99% (or, at the election of such purchaser, 9.99%) of the outstanding share capital of the Company following the consummation of the Registered Direct Offering. Each Pre-Funded Warrant represented the right to purchase one Class A Ordinary Share at an exercise price of $0.0001 per share. The Pre-Funded Warrants were exercisable immediately and at any time until the Pre-Funded Warrants were exercised in full (subject to the beneficial ownership limitation described above). On July 25, 2025, the Pre-Funded Warrants were exercised in full by the Purchaser.

 

The Common Warrants have an exercise price of $2.50 per share, are immediately exercisable upon issuance and have a term of five years from issuance. The Common Warrants (including the Class A Ordinary Shares issuable upon exercise, as applicable) (the “Private Securities”) were issued in reliance upon the exemption from registration pursuant to Section 4(a)(2) under the Securities Act of 1933 (the “Securities Act”) and Regulation D under the Securities Act. The sale of the Private Securities did not involve a public offering and was made without general solicitation or general advertising. Accordingly, the Private Securities have not been registered under the Securities Act or any state securities laws and such securities may not be offered or sold in the United States absent registration, or an exemption from registration, under the Securities Act and any applicable state securities laws. A holder of Common Warrants will have the right to exercise the Common Warrants on a “cashless” basis if there is no effective registration statement registering the resale of the Class A Ordinary Shares underlying the Common Warrants. Subject to limited exceptions, a holder of Common Warrants will not have the right to exercise any portion of its Common Warrants if the holder, together with its affiliates, would beneficially own in excess of 4.99% (or 9.99% at the election of the holder prior to the date of issuance) of the number of Class A Ordinary Shares outstanding immediately after giving effect to such exercise, provided that the holder may increase or decrease the beneficial ownership limitation up to 9.99%. Any increase in the beneficial ownership limitation shall not be effective until 61 days following notice of such change to the Company.

  

The Purchase Agreement contains customary representations, warranties and agreements by the Company, customary conditions to closing, indemnification obligations of the Company, other obligations of the parties, and termination provisions. Additionally, each of the directors and executive officers of the Company entered into a lock-up agreement, pursuant to which they agreed not to sell or transfer any of the Company securities which they hold, subject to certain customary exceptions, during the one hundred twenty (120) day period following the closing of the Registered Direct Offering and concurrent private placement. In addition, the Company agreed (i) to be prohibited from effecting or entering into an agreement to effect any issuance by the Company or any of its subsidiaries of Class A Ordinary Shares or Class A Ordinary Share Equivalents (as defined in the Purchase Agreement) involving a Variable Rate Transaction (as defined in the Purchase Agreement) during the ninety (90) day period after the closing of the Registered Direct Offering and concurrent private placement; (ii) not to issue or enter into any agreement to issue or announce the issuance or proposed issuance of any Class A Ordinary Shares or Ordinary Share Equivalents (as defined in the Purchase Agreement) or file any registration statement or any amendment or supplement thereto, except as set forth in the Prospectus Supplement (defined below), or the Purchase Agreement during the forty five (45) day period following the closing of the Registered Direct Offering and concurrent private placement.

 

1

 

 

The Shares, the Pre-Funded Warrants and the Class A Ordinary Shares underlying the Pre-Funded Warrants were offered by the Company pursuant to a registration statement on Form F-3 (File No.333-282901) (the “Registration Statement”), previously filed and declared effective by the U.S Securities and Exchange Commission (the “Commission”) on November 8, 2024, the base prospectus filed as part of the Registration Statement, and the prospectus supplement dated July 24, 2025 (the “Prospectus Supplement”).

 

On July 24, 2025, the Company entered into a placement agency agreement (the “Placement Agency Agreement”) with Maxim Group LLC (“Maxim” or the “Placement Agent”), pursuant to which the Company engaged Maxim as the exclusive placement agent in connection with the Registered Direct Offering and concurrent private placement. The Placement Agent agreed to use its reasonable best efforts to arrange for the sale of the Shares, the Pre-Funded Warrants and the Common Warrants. In addition, under the Placement Agency Agreement, the Company agreed to pay the Placement Agent a placement agent fee in cash equal to seven percent (7.0%) of the aggregate gross proceeds raised from the sale. The Company also agreed to reimburse the Placement Agent for its out-of-pocket expenses in connection with the Registered Direct Offering and concurrent private placement in an amount not to exceed $40,000.

  

The foregoing summaries of the Pre-Funded Warrants, the Common Warrants, the Placement Agency Agreement, and the Purchase Agreement do not purport to be complete and are subject to, and qualified in their entirety by, such documents filed as Exhibits 4.1, 4.2, 10.1, and 10.2, respectively, hereto and incorporated by reference herein. A copy of the press release related to the Registered Direct Offering and concurrent private placement entitled “U Power Announces Pricing of $1.4 Million Registered Direct Offering” is furnished as Exhibit 99.1 hereto and is incorporated by reference herein.

 

Copies of the opinions of Maples and Calder (Hong Kong) LLP and Hunter Taubman Fischer & Li LLC relating to the legality of the issuance and sale of the Shares, the Pre-Funded Warrants and the Common Warrants, respectively, are filed as Exhibits 5.1 and 5.2 hereto, respectively.

 

This Report is incorporated by reference into the registration statement on Form F-3 (File No. 333-282901) of the Company, filed with the Commission, to be a part thereof from the date on which this report is submitted, to the extent not superseded by documents or reports subsequently filed or furnished.

 

This Report shall not constitute an offer to sell any securities or a solicitation of an offer to buy any securities, nor shall there be any sale of any securities in any state or jurisdiction in which such an offer, solicitation or sale would be unlawful prior to registration or qualification under the securities laws of any such state or jurisdiction.

 

Forward-Looking Statements:

 

This Report contains forward-looking statements within the meaning of the “safe harbor” provisions of the Private Securities Litigation Reform Act of 1995 and other Federal securities laws. All statements other than statements of historical facts included in this Report are forward-looking statements. Forward-looking statements are neither historical facts nor assurances of future performance. Instead, they are based only on the Company’s current beliefs, expectations and assumptions regarding the future of its business, future plans and strategies, projections, anticipated events and trends, the economy and other future conditions. Because forward-looking statements relate to the future, they are subject to inherent uncertainties, risks and changes in circumstances that are difficult to predict and many of which are outside of the Company’s control. The Company’s actual results and financial condition may differ materially from those indicated in the forward-looking statements. Therefore, you should not rely on any of these forward-looking statements. Important factors that could cause our actual results and financial condition to differ materially from those indicated in the forward-looking statements include the risks and uncertainties described in the Company’s annual report on Form 20-F for the year ended December 31, 2024, filed with the Commission on May 15, 2025, and the Company’s other filings with the Commission. The Company undertakes no obligation to publicly update any forward-looking statement, whether written or oral, that may be made from time to time, whether as a result of new information, future developments or otherwise.

 

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Exhibit Index

 

Exhibit No.   Description
4.1   Form of Pre-Funded Warrant
4.2   Form of Common Warrant
5.1   Opinion of Maples and Calder (Hong Kong) LLP
5.2   Opinion of Hunter Taubman Fischer & Li LLC
10.1   Placement Agency Agreement, dated July 24, 2025, by and between the Company and Maxim Group LLC
10.2   Form of Securities Purchase Agreement, dated July 24, 2025, by and between the Company and the purchaser thereto
23.1   Consent of Maples and Calder (Hong Kong) LLP (included in Exhibit 5.1)
23.2   Consent of Hunter Taubman Fischer & Li LLC (included in Exhibit 5.2)
99.1   Press Release on Pricing of the Company’s Registered Direct Offering

 

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SIGNATURE

 

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

 

  U Power Limited
   
  By: /s/ Jia Li
  Name:  Jia Li
  Title: Chief Executive Officer

 

Date: July 28, 2025

 

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FAQ

What regulatory setback did Alvotech (ALVO) disclose in the July 2025 6-K?

The FDA issued a Form 483 after a 26 Jun–4 Jul pre-approval inspection of the Reykjavik plant, noting quality-system deficiencies.

How much capital did Alvotech raise through recent share offerings?

Alvotech raised SEK 39 m via an SDR IPO and SEK 750 m through a private placement in June 2025.

What are the financial terms of the amended term-loan facility?

Post-amendment, the entire $1.081 bn facility bears SOFR + 6.0% cash interest, 50 bp lower than before, maturing July 2029.

Which pipeline assets received positive European feedback?

AVT06 (biosimilar to Eylea) received a positive CHMP opinion, and AVT23 (Xolair) met its primary endpoint in a confirmatory study.

What is the potential value of the expanded Advanz Pharma partnership?

The agreement includes up to €160 m in development and commercial milestones plus revenue sharing.
U Power Limited

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