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[8-K] Upland Software, Inc. Reports Material Event

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(Moderate)
Filing Sentiment
(Neutral)
Form Type
8-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 illustra le azioni di governance, commerciali, regolatorie e finanziarie dall’ultimo rapporto trimestrale.

  • Governance: Sei amministratori rieletti; la veterana Linda Jónsdóttir nominata CFO; il COO Faysal Kalmoua lascia consiglio e management.
  • Commerciale: Collaborazione con Advanz Pharma ampliata a tre nuovi biosimilari (milestone fino a 160 milioni di €) e accordo separato per AVT10 (Cimzia); co-sviluppo globale del biosimilare di Keytruda con Dr. Reddy’s.
  • M&A: Acquisiti il confezionatore svizzero Ivers-Lee e il team R&D svedese di Xbrane, oltre al candidato Cimzia per 275 milioni di corone svedesi.
  • Pipeline: Opinione positiva CHMP per AVT06 (Eylea); studio su AVT23 (Xolair) conferma equivalenza terapeutica.
  • Rischio manifatturiero: Ispezione FDA pre-approvazione (26 giugno–4 luglio) con Form 483 per carenze operative, documentali e di controllo qualità; risposta dettagliata inviata il 25 luglio.
  • Finanziamenti: IPO SDR sovraccapitalizzata (39 milioni SEK) e collocamento istituzionale (750 milioni SEK) aggiungono oltre 3.000 nuovi azionisti; modifica del prestito a termine che annulla la seconda tranche, riduce margine a SOFR+6,0%, linea ora a 1,081 miliardi $ e liquidità 152 milioni $.

Il nuovo capitale e le partnership rafforzano le prospettive di crescita, ma la risoluzione delle questioni regolatorie è cruciale per le approvazioni BLA a breve termine.

El Formulario 6-K de Alvotech de julio de 2025 detalla 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 abandona la junta y la dirección.
  • 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.
  • M&A: Adquirido el empaquetador suizo Ivers-Lee y el equipo de I+D sueco de Xbrane, además del candidato Cimzia por 275 millones de coronas suecas.
  • Pipeline: Opinión positiva del CHMP para AVT06 (Eylea); estudio de AVT23 (Xolair) muestra equivalencia terapéutica.
  • Riesgo de fabricación: Inspección previa a la aprobación de la FDA (26 jun–4 jul) emitió Form 483 señalando deficiencias operativas, documentales y de control de calidad; respuesta detallada presentada el 25 de julio.
  • Financiamiento: IPO SDR sobresuscrita (39 millones SEK) y colocación institucional (750 millones SEK) añaden más de 3,000 nuevos accionistas; enmienda del préstamo a plazo que elimina la segunda tranche, reduce margen a SOFR+6.0%, línea ahora de $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 재무 활동을 상세히 설명합니다.

  • 거버넌스: 6명의 이사 재선임; 베테랑 임원 Linda Jónsdóttir CFO로 임명; COO Faysal Kalmoua는 이사회 및 경영진에서 퇴임.
  • 상업: Advanz Pharma와의 파트너십이 3개의 신규 바이오시밀러(최대 €1억 6천만 마일스톤) 및 별도의 AVT10(Cimzia) 계약으로 확대; Dr. Reddy’s와 Keytruda 바이오시밀러 글로벌 공동개발.
  • M&A: 스위스 포장업체 Ivers-Lee와 Xbrane의 스웨덴 R&D 팀, 그리고 Cimzia 후보를 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 지적한 Form 483 발행; 7월 25일 상세 답변 제출.
  • 재무: SDR IPO(3,900만 SEK) 및 기관 배정(7억 5,000만 SEK) 초과 청약으로 3,000명 이상 신규 주주 확보; 만기 대출 수정으로 두 번째 트랜치 취소, 마진 SOFR+6.0%로 축소, 시설 규모 10억 8,100만 달러, 현금 1억 5,200만 달러.

신규 자본과 파트너십은 성장 전망을 높이지만, 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 cadre expérimentée Linda Jónsdóttir nommée CFO ; le COO Faysal Kalmoua quitte le conseil et la direction.
  • Commercial : Partenariat avec Advanz Pharma élargi à trois nouveaux biosimilaires (jalons jusqu’à 160 M€) et accord séparé pour AVT10 (Cimzia) ; co-développement mondial du biosimilaire de Keytruda avec Dr. Reddy’s.
  • M&A : Acquisition du conditionneur suisse Ivers-Lee et de l’équipe R&D suédoise de Xbrane, ainsi que du candidat Cimzia pour 275 MSEK.
  • Pipeline : Avis positif du CHMP pour AVT06 (Eylea) ; étude AVT23 (Xolair) démontrant une équivalence thérapeutique.
  • Risque de fabrication : Inspection pré-approbation de la FDA (26 juin–4 juillet) ayant émis un Form 483 pour 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 ; modification du prêt à terme annulant la deuxième tranche, réduisant la marge à SOFR+6,0 %, facilité désormais à 1,081 Md$ et trésorerie à 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.

Alvotechs Form 6-K von 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.
  • Kommerzielles: Partnerschaft mit Advanz Pharma auf drei neue Biosimilars ausgeweitet (Meilensteine bis zu 160 Mio. €) sowie separater AVT10 (Cimzia) Vertrag; 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 des Cimzia-Kandidaten für 275 Mio. SEK.
  • Pipeline: Positive CHMP-Stellungnahme zu AVT06 (Eylea); AVT23 (Xolair)-Studie bestätigt therapeutische Äquivalenz.
  • Herstellungsrisiko: FDA-Vorabinspektion (26. Juni–4. Juli) mit Form 483, das operative, dokumentarische und Qualitätskontrollmängel feststellt; detaillierte Antwort am 25. Juli eingereicht.
  • Finanzierung: Überzeichnetes SDR-IPO (39 Mio. SEK) und institutionelle Platzierung (750 Mio. SEK) bringen über 3.000 neue Anteilseigner; Änderung des Terminkredits hebt zweite Tranche auf, senkt Marge auf SOFR+6,0 %, Kreditlinie jetzt 1,081 Mrd. USD, Cash 152 Mio. USD.

Neues Kapital und Partnerschaften verbessern 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 illustra le azioni di governance, commerciali, regolatorie e finanziarie dall’ultimo rapporto trimestrale.

  • Governance: Sei amministratori rieletti; la veterana Linda Jónsdóttir nominata CFO; il COO Faysal Kalmoua lascia consiglio e management.
  • Commerciale: Collaborazione con Advanz Pharma ampliata a tre nuovi biosimilari (milestone fino a 160 milioni di €) e accordo separato per AVT10 (Cimzia); co-sviluppo globale del biosimilare di Keytruda con Dr. Reddy’s.
  • M&A: Acquisiti il confezionatore svizzero Ivers-Lee e il team R&D svedese di Xbrane, oltre al candidato Cimzia per 275 milioni di corone svedesi.
  • Pipeline: Opinione positiva CHMP per AVT06 (Eylea); studio su AVT23 (Xolair) conferma equivalenza terapeutica.
  • Rischio manifatturiero: Ispezione FDA pre-approvazione (26 giugno–4 luglio) con Form 483 per carenze operative, documentali e di controllo qualità; risposta dettagliata inviata il 25 luglio.
  • Finanziamenti: IPO SDR sovraccapitalizzata (39 milioni SEK) e collocamento istituzionale (750 milioni SEK) aggiungono oltre 3.000 nuovi azionisti; modifica del prestito a termine che annulla la seconda tranche, riduce margine a SOFR+6,0%, linea ora a 1,081 miliardi $ e liquidità 152 milioni $.

Il nuovo capitale e le partnership rafforzano le prospettive di crescita, ma la risoluzione delle questioni regolatorie è cruciale per le approvazioni BLA a breve termine.

El Formulario 6-K de Alvotech de julio de 2025 detalla 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 abandona la junta y la dirección.
  • 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.
  • M&A: Adquirido el empaquetador suizo Ivers-Lee y el equipo de I+D sueco de Xbrane, además del candidato Cimzia por 275 millones de coronas suecas.
  • Pipeline: Opinión positiva del CHMP para AVT06 (Eylea); estudio de AVT23 (Xolair) muestra equivalencia terapéutica.
  • Riesgo de fabricación: Inspección previa a la aprobación de la FDA (26 jun–4 jul) emitió Form 483 señalando deficiencias operativas, documentales y de control de calidad; respuesta detallada presentada el 25 de julio.
  • Financiamiento: IPO SDR sobresuscrita (39 millones SEK) y colocación institucional (750 millones SEK) añaden más de 3,000 nuevos accionistas; enmienda del préstamo a plazo que elimina la segunda tranche, reduce margen a SOFR+6.0%, línea ahora de $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 재무 활동을 상세히 설명합니다.

  • 거버넌스: 6명의 이사 재선임; 베테랑 임원 Linda Jónsdóttir CFO로 임명; COO Faysal Kalmoua는 이사회 및 경영진에서 퇴임.
  • 상업: Advanz Pharma와의 파트너십이 3개의 신규 바이오시밀러(최대 €1억 6천만 마일스톤) 및 별도의 AVT10(Cimzia) 계약으로 확대; Dr. Reddy’s와 Keytruda 바이오시밀러 글로벌 공동개발.
  • M&A: 스위스 포장업체 Ivers-Lee와 Xbrane의 스웨덴 R&D 팀, 그리고 Cimzia 후보를 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 지적한 Form 483 발행; 7월 25일 상세 답변 제출.
  • 재무: SDR IPO(3,900만 SEK) 및 기관 배정(7억 5,000만 SEK) 초과 청약으로 3,000명 이상 신규 주주 확보; 만기 대출 수정으로 두 번째 트랜치 취소, 마진 SOFR+6.0%로 축소, 시설 규모 10억 8,100만 달러, 현금 1억 5,200만 달러.

신규 자본과 파트너십은 성장 전망을 높이지만, 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 cadre expérimentée Linda Jónsdóttir nommée CFO ; le COO Faysal Kalmoua quitte le conseil et la direction.
  • Commercial : Partenariat avec Advanz Pharma élargi à trois nouveaux biosimilaires (jalons jusqu’à 160 M€) et accord séparé pour AVT10 (Cimzia) ; co-développement mondial du biosimilaire de Keytruda avec Dr. Reddy’s.
  • M&A : Acquisition du conditionneur suisse Ivers-Lee et de l’équipe R&D suédoise de Xbrane, ainsi que du candidat Cimzia pour 275 MSEK.
  • Pipeline : Avis positif du CHMP pour AVT06 (Eylea) ; étude AVT23 (Xolair) démontrant une équivalence thérapeutique.
  • Risque de fabrication : Inspection pré-approbation de la FDA (26 juin–4 juillet) ayant émis un Form 483 pour 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 ; modification du prêt à terme annulant la deuxième tranche, réduisant la marge à SOFR+6,0 %, facilité désormais à 1,081 Md$ et trésorerie à 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.

Alvotechs Form 6-K von 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.
  • Kommerzielles: Partnerschaft mit Advanz Pharma auf drei neue Biosimilars ausgeweitet (Meilensteine bis zu 160 Mio. €) sowie separater AVT10 (Cimzia) Vertrag; 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 des Cimzia-Kandidaten für 275 Mio. SEK.
  • Pipeline: Positive CHMP-Stellungnahme zu AVT06 (Eylea); AVT23 (Xolair)-Studie bestätigt therapeutische Äquivalenz.
  • Herstellungsrisiko: FDA-Vorabinspektion (26. Juni–4. Juli) mit Form 483, das operative, dokumentarische und Qualitätskontrollmängel feststellt; detaillierte Antwort am 25. Juli eingereicht.
  • Finanzierung: Überzeichnetes SDR-IPO (39 Mio. SEK) und institutionelle Platzierung (750 Mio. SEK) bringen über 3.000 neue Anteilseigner; Änderung des Terminkredits hebt zweite Tranche auf, senkt Marge auf SOFR+6,0 %, Kreditlinie jetzt 1,081 Mrd. USD, Cash 152 Mio. USD.

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

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UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, DC 20549
FORM 8-K
CURRENT REPORT
Pursuant to Section 13 or 15(d) of
The Securities Exchange Act of 1934
July 25, 2025
Date of Report (Date of earliest event reported)
UPLAND SOFTWARE, INC.
(Exact name of registrant as specified in its charter)
Delaware001-3672027-2992077
(State or other jurisdiction of incorporation)(Commission File Number)(IRS Employer Identification No.)
900 S. Capital of Texas Highway, Las Cimas IV Suite 300
Austin, Texas 78746
(Address of principal executive offices, including zip code)
(512) 960-1010
(Registrant’s telephone number, including area code)
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 classTrading SymbolName of each exchange on which registered
Common Stock, par value $0.0001 per shareUPLDThe Nasdaq Global Market
Preferred Stock Purchase Rights-The Nasdaq Global Market
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 25, 2025 (the “Closing Date”), Upland Software, Inc. (“Upland”) and certain of its subsidiaries (together with Upland, the “Companies”) entered into a Credit Agreement (the “Credit Agreement”) with the lenders party thereto and private credit direct lender Sound Point Capital, as administrative agent.
The Credit Agreement established a new senior secured term loan facility in an aggregate principal amount of $240 million (the “Term Loan”). On the Closing Date, Upland used the proceeds from the Term Loan, together with cash on hand, to redeem all of the $258 million outstanding aggregate principal amount of Upland’s previous senior secured credit facility.
The Term Loan will mature on July 25, 2031 and bear an interest rate of the secured overnight financing rate, which shall not be less than 1.50%, plus a margin of 6.00% per annum (with step downs and a potential step up at specified leverage levels). The Term Loan also includes (i) a covenant tested quarterly which limits the consolidated secured leverage ratio to 6.0 to 1.0 or under and (ii) certain other changes to the terms of the Credit Agreement, including with respect to certain negative covenants. Payments on the Term Loan will be due quarterly in amounts equal to (a) 2.50% per annum of the original principal amount of the Term Loan commencing beginning December 31, 2025 through September 30, 2026, (b) 1.75% per annum of the original principal amount of the Term Loan commencing December 31, 2026 through September 30, 2027, and (c) 1.00% per annum of the original principal amount of the Term Loan commencing December 31, 2027 and continuing each fiscal quarter thereafter, with the balance payable on the final maturity date.
In addition to the Term Loan, the Credit Agreement provides for a $30 million senior secured revolving credit facility (the “Revolving Facility” and together with the Term Loan, the “Credit Facilities”). The Revolving Facility will mature on July 25, 2031 and will bear the same interest rate as the Term Loan. The Revolving Facility will be subject to the same covenants and terms as the Term Loan. The proceeds of loans under the Revolving Facility will be used by Upland from time to time after the Closing Date for working capital and other general corporate purposes.
The Credit Agreement contains customary representations, warranties, affirmative and negative covenants, including a financial covenant, and events of default. Obligations under the Credit Agreement are secured by substantially all of the Company’s assets, subject to certain exclusions.
The foregoing description of the Credit Agreement does not purport to be complete and is qualified in its entirety by reference to the Credit Agreement, which is filed hereto as Exhibit 10.1 and is incorporated by reference herein.

Item 2.03. Creation of Direct Financial Obligation.
The information included under Item 1.01 above regarding the Credit Agreement is incorporated by reference into this Item 2.03.

Item 8.01. Other Events.
On July 28, 2025, Upland issued a press release announcing that it had closed the Credit Agreement. The press release is filed hereto as Exhibit 99.1 and is incorporated by reference herein.



Item 9.01      Financial Statements and Exhibits.
(d) Exhibits.
Exhibit No.
 Description
10.1*
Credit Agreement, dated as of July 25, 2025, by and among Upland Software, Inc., the subsidiary guarantors party thereto, Sound Point Capital, as administrative agent, and the lenders party thereto.
99.1
Press Release of Upland Software, Inc. dated July 28, 2025
104The cover page from this Current Report on Form 8-K, formatted as Inline XBRL
* Certain schedules and similar attachments have been omitted pursuant to Item 601(a)(5) of Regulation S-K. Upland Software, Inc. hereby undertakes to furnish supplemental copies of such schedules and attachments to the Securities and Exchange Commission upon request.



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.
UPLAND SOFTWARE, INC.
By:/s/ Michael D. Hill
Michael D. Hill
Chief Financial Officer
Date: July 28, 2025


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.
Upland Software

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