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[S-8] 8x8, Inc. Employee Benefit Plan Registration

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(No impact)
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(Neutral)
Form Type
S-8
Rhea-AI Filing Summary

Q2-25 headline: Net revenue $150.0 M (+72% YoY) driven by Auvelity, Sunosi and first weeks of Symbravo launch; GAAP net loss narrowed to $48.0 M (-39% YoY) or �$0.97/sh.

Six-month revenue reached $271.5 M (+67%) while loss trimmed to $107.4 M. Gross margin remained high (cost of revenue �9% of sales), but SG&A climbed 26% to $130.3 M as Axsome expanded its commercial footprint. R&D held steady at $49.5 M with multiple late-stage CNS programs in progress.

Cash & equivalents closed at $303.0 M; operating cash burn fell to $75.8 M. In May the company refinanced via a new $570 M facility with Blackstone: $120 M term loan and $70 M revolver drawn, retiring the costlier Hercules loan and expected to lower interest expense; Blackstone also invested $15 M in common stock. Total debt now $188 M, shareholders� equity $73 M.

FDA approved migraine therapy Symbravo in Jan-25 with U.S. launch in June, giving Axsome three commercial products. Management believes current liquidity funds operations for at least 12 months. Key risks are sustained commercial uptake, sizable rebates/discounts ($118 M accrued), and ongoing operating losses.

Titolo Q2-25: Ricavi netti di 150,0 milioni di dollari (+72% su base annua) trainati da Auvelity, Sunosi e dalle prime settimane del lancio di Symbravo; la perdita netta GAAP si è ridotta a 48,0 milioni di dollari (-39% su base annua) ovvero -0,97 dollari per azione.

I ricavi semestrali hanno raggiunto 271,5 milioni di dollari (+67%) mentre la perdita si è ridotta a 107,4 milioni. Il margine lordo è rimasto elevato (costo del venduto �9% delle vendite), ma le spese SG&A sono aumentate del 26% a 130,3 milioni, in seguito all'espansione della presenza commerciale di Axsome. La R&S è rimasta stabile a 49,5 milioni con diversi programmi CNS in fase avanzata in corso.

La liquidità e equivalenti si sono attestati a 303,0 milioni; il consumo di cassa operativo è sceso a 75,8 milioni. A maggio la società ha rifinanziato tramite una nuova linea da 570 milioni con Blackstone: un prestito a termine da 120 milioni e una linea revolving da 70 milioni utilizzata, estinguendo il più costoso prestito Hercules e prevedendo una riduzione delle spese per interessi; Blackstone ha inoltre investito 15 milioni in azioni ordinarie. Il debito totale è ora di 188 milioni, il patrimonio netto degli azionisti di 73 milioni.

La FDA ha approvato a gennaio 2025 la terapia per l'emicrania Symbravo, con lancio negli Stati Uniti a giugno, portando a tre i prodotti commerciali di Axsome. La direzione ritiene che la liquidità attuale copra le operazioni per almeno 12 mesi. I rischi principali sono il mantenimento delle vendite commerciali, significativi rimborsi/sconti accumulati (118 milioni) e le perdite operative in corso.

Titular Q2-25: Ingresos netos de 150,0 millones de dólares (+72% interanual) impulsados por Auvelity, Sunosi y las primeras semanas del lanzamiento de Symbravo; la pérdida neta GAAP se redujo a 48,0 millones de dólares (-39% interanual) o -0,97 dólares por acción.

Los ingresos a seis meses alcanzaron 271,5 millones (+67%), mientras que la pérdida se redujo a 107,4 millones. El margen bruto se mantuvo alto (costo de ventas �9% de las ventas), pero los gastos SG&A aumentaron un 26% a 130,3 millones debido a la expansión comercial de Axsome. I+D se mantuvo estable en 49,5 millones con varios programas CNS en etapas avanzadas en curso.

El efectivo y equivalentes cerraron en 303,0 millones; el consumo de efectivo operativo cayó a 75,8 millones. En mayo, la compañía refinanció mediante una nueva línea de 570 millones con Blackstone: un préstamo a plazo de 120 millones y una línea revolvente de 70 millones utilizada, cancelando el préstamo más costoso de Hercules y esperando reducir los gastos por intereses; Blackstone también invirtió 15 millones en acciones comunes. La deuda total ahora es de 188 millones, el patrimonio de los accionistas de 73 millones.

La FDA aprobó en enero de 2025 la terapia para migraña Symbravo, con lanzamiento en EE.UU. en junio, dando a Axsome tres productos comerciales. La dirección considera que la liquidez actual financia las operaciones al menos por 12 meses. Los riesgos clave son la sostenida adopción comercial, reembolsos/descuentos significativos acumulados (118 millones) y las pérdidas operativas continuas.

Q2-25 헤드ë¼ì¸: Auvelity, Sunosi ë°� Symbravo 출시 초기 주간ì—� 힘입ì–� 순매ì¶� 1ì–� 5천만 달러(+72% ì „ë…„ 대ë¹�) 기ë¡; GAAP 순ì†ì‹¤ì€ 4,800ë§� 달러(-39% ì „ë…„ 대ë¹�) ë˜ëŠ” 주당 -0.97달러ë¡� 축소ë�.

6개월 ë§¤ì¶œì€ 2ì–� 7,150ë§� 달러(+67%)ì—� 달했ê³� ì†ì‹¤ì€ 1ì–� 740ë§� 달러ë¡� 줄어ë“�. ì´ì´ìµë¥ ì€ 높게 유지(매출ì›ê°€ ì•� 9%) ë˜ì—ˆìœ¼ë‚˜, Axsomeì� ì˜ì—… 확장으로 íŒë§¤ê´€ë¦¬ë¹„(SG&A)ëŠ� 1ì–� 3,030ë§� 달러ë¡� 26% ì¦ê°€. 연구개발ë¹�(R&D)ëŠ� 4,950ë§� 달러ë¡� 안정ì ì´ë©� 여러 후기 중추신경ê³�(CNS) 프로그램ì� ì§„í–‰ ì¤�.

현금 ë°� 현금ì„� ìžì‚°ì€ 3ì–� 300ë§� 달러ë¡� 마ê°; ì˜ì—…현금 소모ëŠ� 7,580ë§� 달러ë¡� ê°ì†Œ. 5ì›”ì— Blackstoneê³� 5ì–� 7,000ë§� 달러 규모ì� ì‹ ê·œ 금융계약ì� 통해 재융ìž�: 1ì–� 2,000ë§� 달러ì� 기한부 대출과 7,000ë§� 달러ì� 리볼ë¹� 대ì¶� 사용, ë� 비용ì� ë†’ì€ Hercules 대ì¶� ìƒí™˜ ë°� ì´ìž 비용 ì ˆê° ê¸°ëŒ€; Blackstoneì€ ë³´í†µì£¼ì— 1,500ë§� 달러ë� 투ìž. ì´� 부채는 현재 1ì–� 8,800ë§� 달러, 주주 ì§€ë¶„ì€ 7,300ë§� 달러.

FDAëŠ� 2025ë…� 1ì›”ì— íŽ¸ë‘í†� 치료ì � Symbravoë¥� 승ì¸í–ˆìœ¼ë©�, 6ì›� 미국 출시ë¡� Axsomeì€ 3ê°œì˜ ìƒì—… 제품ì� 보유. ê²½ì˜ì§„ì€ í˜„ìž¬ 유ë™ì„±ì´ 최소 12개월ê°� ìš´ì˜ ìžê¸ˆì� ì§€ì›í•  것으ë¡� ë³´ê³  있ìŒ. 주요 ìœ„í—˜ì€ ì§€ì†ì ì� ìƒì—…ì � 수요, ìƒë‹¹í•� 리베ì´íЏ/í• ì¸(1ì–� 1,800ë§� 달러 ë°œìƒ) ë°� ì§€ì†ì ì� ìš´ì˜ ì†ì‹¤.

Titre Q2-25 : Chiffre d'affaires net de 150,0 M$ (+72% en glissement annuel) porté par Auvelity, Sunosi et les premières semaines du lancement de Symbravo ; la perte nette selon les normes GAAP s'est réduite à 48,0 M$ (-39% en glissement annuel) soit -0,97 $/action.

Le chiffre d'affaires sur six mois a atteint 271,5 M$ (+67%) tandis que la perte a été réduite à 107,4 M$. La marge brute est restée élevée (coût des ventes �9% des ventes), mais les frais SG&A ont augmenté de 26% pour atteindre 130,3 M$ suite à l'expansion commerciale d'Axsome. La R&D est restée stable à 49,5 M$ avec plusieurs programmes CNS en phase avancée en cours.

La trésorerie et équivalents s'élèvent à 303,0 M$ ; la consommation de trésorerie opérationnelle est tombée à 75,8 M$. En mai, la société a refinancé via une nouvelle facilité de 570 M$ avec Blackstone : un prêt à terme de 120 M$ et une ligne de crédit renouvelable de 70 M$ utilisée, remboursant le prêt plus coûteux Hercules et prévoyant une réduction des charges d'intérêts ; Blackstone a également investi 15 M$ en actions ordinaires. La dette totale est désormais de 188 M$, les capitaux propres des actionnaires de 73 M$.

La FDA a approuvé en janvier 2025 la thérapie contre la migraine Symbravo, lancée aux États-Unis en juin, portant à trois le nombre de produits commerciaux d'Axsome. La direction estime que la liquidité actuelle finance les opérations pour au moins 12 mois. Les principaux risques sont une adoption commerciale soutenue, des remises/ristournes importantes accumulées (118 M$) et des pertes opérationnelles continues.

Q2-25 Überschrift: Nettoumsatz 150,0 Mio. $ (+72% im Jahresvergleich) getrieben von Auvelity, Sunosi und den ersten Wochen des Symbravo-Starts; GAAP-Nettogewinnrückgang auf 48,0 Mio. $ (-39% im Jahresvergleich) bzw. �0,97 $/Aktie.

Sechsmonatsumsatz erreichte 271,5 Mio. $ (+67%), während der Verlust auf 107,4 Mio. $ reduziert wurde. Bruttomarge blieb hoch (Kosten der Umsatzerlöse �9% des Umsatzes), aber SG&A stiegen um 26% auf 130,3 Mio., da Axsome seine kommerzielle Präsenz ausbaute. F&E blieb mit 49,5 Mio. stabil, mehrere späte CNS-Programme laufen.

Barmittel und Äquivalente schlossen bei 303,0 Mio.; operativer Cashburn fiel auf 75,8 Mio. Im Mai refinanzierte das Unternehmen über eine neue 570-Mio.-$-Fazilität mit Blackstone: 120 Mio. $ Terminkredit und 70 Mio. $ revolvierender Kredit gezogen, wodurch der teurere Hercules-Kredit abgelöst und Zinskosten voraussichtlich gesenkt werden; Blackstone investierte zudem 15 Mio. $ in Stammaktien. Gesamtschulden nun 188 Mio., Eigenkapital der Aktionäre 73 Mio.

Die FDA genehmigte im Januar 2025 die Migränetherapie Symbravo, Markteinführung in den USA im Juni, womit Axsome drei kommerzielle Produkte besitzt. Das Management geht davon aus, dass die aktuelle Liquidität den Betrieb mindestens 12 Monate finanziert. Wesentliche Risiken sind nachhaltige Marktdurchdringung, beträchtliche Rückerstattungen/Rabatte (118 Mio. $ gebildet) und fortlaufende operative Verluste.

Positive
  • Revenue surged 72% YoY to $150.0 M, reflecting robust uptake of Auvelity/Sunosi and initial Symbravo sales.
  • Net loss narrowed 39% YoY to $48.0 M, improving EPS to â€�$0.97 from â€�$1.67.
  • Blackstone $570 M financing refinanced higher-cost debt, expected to reduce interest expense and offers additional $250 M optional capital.
  • Healthy liquidity of $303 M plus new facility supports â‰�12-month operating runway.
  • FDA approval & June launch of Symbravo adds a third revenue stream and diversifies the portfolio.
Negative
  • Company remains unprofitable with operating loss of $36.7 M and accumulated deficit of $1.23 B.
  • SG&A rose 26% YoY to $130.3 M, outpacing revenue growth and pressuring margins.
  • Total debt increased to $188 M after new borrowings; leverage must be managed.
  • High gross-to-net deductions with rebates/discounts liability climbing to $118 M, eroding realized pricing.
  • Shareholdersâ€� equity only $73 M, indicating a highly leveraged balance sheet relative to equity.

Insights

TL;DR: Strong top-line growth and lower cost debt extend runway, but profit inflection still unclear.

Revenue momentum is impressive—Auvelity and Sunosi grew sharply and Symbravo adds a new lever. Gross margin held near 90%, evidencing product pricing power. The Blackstone facility replaces higher-rate Hercules debt, cutting the effective rate to SOFR+4.75% and deferring large amortization until 2030, a cash-flow win. Yet SG&A inflation outpaced sales (up 26% YoY) as the company ramps three brands, and total operating expenses still exceed revenue by >20%. Net leverage is ~0.3× sales, manageable but worth monitoring given future R&D and launch spend. Path to breakeven likely depends on accelerating Auvelity scripts and rapid Symbravo adoption.

TL;DR: Triple-product portfolio plus cheaper capital signal upside; execution risk remains.

Axsome now markets treatments for depression, sleep disorders and migraine—three distinct, large markets. The 72% YoY revenue jump validates demand and diversifies cash flows. Refinancing with Blackstone frees incremental capital (up to $250 M undrawn) and included an equity buy, aligning lender incentives. Cash of $303 M covers >12 months of forecast burn even before optional draws. If Symbravo repeats Auvelity’s early trajectory, 2026 profitability is plausible. Investors should watch rebate pressure and ensure SG&A efficiencies emerge post-launch curve.

Titolo Q2-25: Ricavi netti di 150,0 milioni di dollari (+72% su base annua) trainati da Auvelity, Sunosi e dalle prime settimane del lancio di Symbravo; la perdita netta GAAP si è ridotta a 48,0 milioni di dollari (-39% su base annua) ovvero -0,97 dollari per azione.

I ricavi semestrali hanno raggiunto 271,5 milioni di dollari (+67%) mentre la perdita si è ridotta a 107,4 milioni. Il margine lordo è rimasto elevato (costo del venduto �9% delle vendite), ma le spese SG&A sono aumentate del 26% a 130,3 milioni, in seguito all'espansione della presenza commerciale di Axsome. La R&S è rimasta stabile a 49,5 milioni con diversi programmi CNS in fase avanzata in corso.

La liquidità e equivalenti si sono attestati a 303,0 milioni; il consumo di cassa operativo è sceso a 75,8 milioni. A maggio la società ha rifinanziato tramite una nuova linea da 570 milioni con Blackstone: un prestito a termine da 120 milioni e una linea revolving da 70 milioni utilizzata, estinguendo il più costoso prestito Hercules e prevedendo una riduzione delle spese per interessi; Blackstone ha inoltre investito 15 milioni in azioni ordinarie. Il debito totale è ora di 188 milioni, il patrimonio netto degli azionisti di 73 milioni.

La FDA ha approvato a gennaio 2025 la terapia per l'emicrania Symbravo, con lancio negli Stati Uniti a giugno, portando a tre i prodotti commerciali di Axsome. La direzione ritiene che la liquidità attuale copra le operazioni per almeno 12 mesi. I rischi principali sono il mantenimento delle vendite commerciali, significativi rimborsi/sconti accumulati (118 milioni) e le perdite operative in corso.

Titular Q2-25: Ingresos netos de 150,0 millones de dólares (+72% interanual) impulsados por Auvelity, Sunosi y las primeras semanas del lanzamiento de Symbravo; la pérdida neta GAAP se redujo a 48,0 millones de dólares (-39% interanual) o -0,97 dólares por acción.

Los ingresos a seis meses alcanzaron 271,5 millones (+67%), mientras que la pérdida se redujo a 107,4 millones. El margen bruto se mantuvo alto (costo de ventas �9% de las ventas), pero los gastos SG&A aumentaron un 26% a 130,3 millones debido a la expansión comercial de Axsome. I+D se mantuvo estable en 49,5 millones con varios programas CNS en etapas avanzadas en curso.

El efectivo y equivalentes cerraron en 303,0 millones; el consumo de efectivo operativo cayó a 75,8 millones. En mayo, la compañía refinanció mediante una nueva línea de 570 millones con Blackstone: un préstamo a plazo de 120 millones y una línea revolvente de 70 millones utilizada, cancelando el préstamo más costoso de Hercules y esperando reducir los gastos por intereses; Blackstone también invirtió 15 millones en acciones comunes. La deuda total ahora es de 188 millones, el patrimonio de los accionistas de 73 millones.

La FDA aprobó en enero de 2025 la terapia para migraña Symbravo, con lanzamiento en EE.UU. en junio, dando a Axsome tres productos comerciales. La dirección considera que la liquidez actual financia las operaciones al menos por 12 meses. Los riesgos clave son la sostenida adopción comercial, reembolsos/descuentos significativos acumulados (118 millones) y las pérdidas operativas continuas.

Q2-25 헤드ë¼ì¸: Auvelity, Sunosi ë°� Symbravo 출시 초기 주간ì—� 힘입ì–� 순매ì¶� 1ì–� 5천만 달러(+72% ì „ë…„ 대ë¹�) 기ë¡; GAAP 순ì†ì‹¤ì€ 4,800ë§� 달러(-39% ì „ë…„ 대ë¹�) ë˜ëŠ” 주당 -0.97달러ë¡� 축소ë�.

6개월 ë§¤ì¶œì€ 2ì–� 7,150ë§� 달러(+67%)ì—� 달했ê³� ì†ì‹¤ì€ 1ì–� 740ë§� 달러ë¡� 줄어ë“�. ì´ì´ìµë¥ ì€ 높게 유지(매출ì›ê°€ ì•� 9%) ë˜ì—ˆìœ¼ë‚˜, Axsomeì� ì˜ì—… 확장으로 íŒë§¤ê´€ë¦¬ë¹„(SG&A)ëŠ� 1ì–� 3,030ë§� 달러ë¡� 26% ì¦ê°€. 연구개발ë¹�(R&D)ëŠ� 4,950ë§� 달러ë¡� 안정ì ì´ë©� 여러 후기 중추신경ê³�(CNS) 프로그램ì� ì§„í–‰ ì¤�.

현금 ë°� 현금ì„� ìžì‚°ì€ 3ì–� 300ë§� 달러ë¡� 마ê°; ì˜ì—…현금 소모ëŠ� 7,580ë§� 달러ë¡� ê°ì†Œ. 5ì›”ì— Blackstoneê³� 5ì–� 7,000ë§� 달러 규모ì� ì‹ ê·œ 금융계약ì� 통해 재융ìž�: 1ì–� 2,000ë§� 달러ì� 기한부 대출과 7,000ë§� 달러ì� 리볼ë¹� 대ì¶� 사용, ë� 비용ì� ë†’ì€ Hercules 대ì¶� ìƒí™˜ ë°� ì´ìž 비용 ì ˆê° ê¸°ëŒ€; Blackstoneì€ ë³´í†µì£¼ì— 1,500ë§� 달러ë� 투ìž. ì´� 부채는 현재 1ì–� 8,800ë§� 달러, 주주 ì§€ë¶„ì€ 7,300ë§� 달러.

FDAëŠ� 2025ë…� 1ì›”ì— íŽ¸ë‘í†� 치료ì � Symbravoë¥� 승ì¸í–ˆìœ¼ë©�, 6ì›� 미국 출시ë¡� Axsomeì€ 3ê°œì˜ ìƒì—… 제품ì� 보유. ê²½ì˜ì§„ì€ í˜„ìž¬ 유ë™ì„±ì´ 최소 12개월ê°� ìš´ì˜ ìžê¸ˆì� ì§€ì›í•  것으ë¡� ë³´ê³  있ìŒ. 주요 ìœ„í—˜ì€ ì§€ì†ì ì� ìƒì—…ì � 수요, ìƒë‹¹í•� 리베ì´íЏ/í• ì¸(1ì–� 1,800ë§� 달러 ë°œìƒ) ë°� ì§€ì†ì ì� ìš´ì˜ ì†ì‹¤.

Titre Q2-25 : Chiffre d'affaires net de 150,0 M$ (+72% en glissement annuel) porté par Auvelity, Sunosi et les premières semaines du lancement de Symbravo ; la perte nette selon les normes GAAP s'est réduite à 48,0 M$ (-39% en glissement annuel) soit -0,97 $/action.

Le chiffre d'affaires sur six mois a atteint 271,5 M$ (+67%) tandis que la perte a été réduite à 107,4 M$. La marge brute est restée élevée (coût des ventes �9% des ventes), mais les frais SG&A ont augmenté de 26% pour atteindre 130,3 M$ suite à l'expansion commerciale d'Axsome. La R&D est restée stable à 49,5 M$ avec plusieurs programmes CNS en phase avancée en cours.

La trésorerie et équivalents s'élèvent à 303,0 M$ ; la consommation de trésorerie opérationnelle est tombée à 75,8 M$. En mai, la société a refinancé via une nouvelle facilité de 570 M$ avec Blackstone : un prêt à terme de 120 M$ et une ligne de crédit renouvelable de 70 M$ utilisée, remboursant le prêt plus coûteux Hercules et prévoyant une réduction des charges d'intérêts ; Blackstone a également investi 15 M$ en actions ordinaires. La dette totale est désormais de 188 M$, les capitaux propres des actionnaires de 73 M$.

La FDA a approuvé en janvier 2025 la thérapie contre la migraine Symbravo, lancée aux États-Unis en juin, portant à trois le nombre de produits commerciaux d'Axsome. La direction estime que la liquidité actuelle finance les opérations pour au moins 12 mois. Les principaux risques sont une adoption commerciale soutenue, des remises/ristournes importantes accumulées (118 M$) et des pertes opérationnelles continues.

Q2-25 Überschrift: Nettoumsatz 150,0 Mio. $ (+72% im Jahresvergleich) getrieben von Auvelity, Sunosi und den ersten Wochen des Symbravo-Starts; GAAP-Nettogewinnrückgang auf 48,0 Mio. $ (-39% im Jahresvergleich) bzw. �0,97 $/Aktie.

Sechsmonatsumsatz erreichte 271,5 Mio. $ (+67%), während der Verlust auf 107,4 Mio. $ reduziert wurde. Bruttomarge blieb hoch (Kosten der Umsatzerlöse �9% des Umsatzes), aber SG&A stiegen um 26% auf 130,3 Mio., da Axsome seine kommerzielle Präsenz ausbaute. F&E blieb mit 49,5 Mio. stabil, mehrere späte CNS-Programme laufen.

Barmittel und Äquivalente schlossen bei 303,0 Mio.; operativer Cashburn fiel auf 75,8 Mio. Im Mai refinanzierte das Unternehmen über eine neue 570-Mio.-$-Fazilität mit Blackstone: 120 Mio. $ Terminkredit und 70 Mio. $ revolvierender Kredit gezogen, wodurch der teurere Hercules-Kredit abgelöst und Zinskosten voraussichtlich gesenkt werden; Blackstone investierte zudem 15 Mio. $ in Stammaktien. Gesamtschulden nun 188 Mio., Eigenkapital der Aktionäre 73 Mio.

Die FDA genehmigte im Januar 2025 die Migränetherapie Symbravo, Markteinführung in den USA im Juni, womit Axsome drei kommerzielle Produkte besitzt. Das Management geht davon aus, dass die aktuelle Liquidität den Betrieb mindestens 12 Monate finanziert. Wesentliche Risiken sind nachhaltige Marktdurchdringung, beträchtliche Rückerstattungen/Rabatte (118 Mio. $ gebildet) und fortlaufende operative Verluste.


As filed with the Securities and Exchange Commission on August 4, 2025
Registration No. 333- _____
UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM
S-8

REGISTRATION STATEMENT

UNDER
THE SECURITIES ACT OF 1933
a8x8-logoxdkgrey.jpg
8x8, INC.
(Exact name of Registrant as Specified in its Charter)
Delaware77-0142404
(State or Other Jurisdiction of Incorporation or Organization) (I.R.S. Employer Identification Number)
675 Creekside Way
Campbell, CA 95008
(Address of principal executive offices)
(408) 727-1885
(Registrant's telephone number, including area code)
8x8, Inc. Amended and Restated 2022 Equity Incentive Plan
8x8, Inc. Amended and Restated 2017 New Employee Inducement Incentive Plan

8x8, Inc. Amended and Restated 1996 Employee Stock Purchase Plan
(Full Title of the Plans)

Laurence Denny
Secretary and Chief Legal Officer
8x8, Inc.
675 Creekside Way
Campbell, CA 95008
(Name and Address of Agent For Service)
(408) 727-1885
(Telephone Number, Including Area Code, of Agent For Service)

Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, a smaller reporting company or an emerging growth company. See the definitions of “large accelerated filer,” “accelerated filer,” “smaller reporting company” and “emerging growth company” in Rule 12b-2 of the Exchange Act.

Large accelerated filerAccelerated filer
Non-accelerated filerSmaller reporting company
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 7(a)(2)(B) of the Securities Act.



INFORMATION REQUIRED PURSUANT
TO GENERAL INSTRUCTION E TO FORM S-8
 
Explanatory Note
 
This Registration Statement on Form S-8 (this "Registration Statement") is being filed by 8x8, Inc. (the “Registrant”) to register (i) an additional 8,500,000 shares of its common stock, $0.001 par value per share (the “Common Stock”), under the Registrant’s Amended and Restated 2022 Equity Incentive Plan (the “2022 Plan”) and an additional 6,000,000 shares of Common Stock under the Registrant’s Amended and Restated 1996 Employee Stock Purchase Plan, in each case, pursuant to amendments to the respective plans authorized and approved by the stockholders of the Registrant on July 25, 2025 and (ii) up to an additional 1,000,000 shares of Common Stock under the Registrant's Amended and Restated 2017 New Employee Inducement Incentive Plan (the "2017 Inducement Plan"), and up to an additional 5,000,000 shares of Common Stock under the 2022 Plan, in each case, to account for shares of Common Stock that have been granted or may be granted and are subsequently cancelled prior to issuance and will be re-issuable to eligible individuals under the 2022 Plan and the 2017 Inducement Plan, respectively.

This Registration Statement hereby incorporates by reference the contents of the Registrant’s applicable previous registration statements on Form S-8 filed with the Securities and Exchange Commission (the "SEC") (File Nos. 333-30943, 333-50519, 333-15627, 333-66296, 333-90172, 333-118642, 333-126337, 333-137599, 333-189452, 333-196275, 333-204583, 333-212163, 333-218472, 333-221290, 333-225388, 333-231670, 333-238572, 333-249757, 333-251489, 333-262510, 333-266171, 333-272218, 333-276829, 333-281756, and 333-284709). Collectively, all prior registration statements referenced above are referred to herein as the “Prior Registration Statements.”

This Registration Statement relates to securities of the same class as that to which the Prior Registration Statements relate and is submitted in accordance with Instruction E to Form S-8 regarding the registration of additional securities. Accordingly, the contents of the Prior Registration Statements are incorporated herein by reference and made part of this Registration Statement, except as amended hereby.

PART II
INFORMATION REQUIRED IN THE REGISTRATION STATEMENT
Item 3.    Incorporation of Documents by Reference.
    The following documents filed by the Registrant with the SEC are hereby incorporated by reference in this Registration Statement:
1.The Registrant’s Annual Report on Form 10-K for the fiscal year ended March 31, 2025, filed with the SEC on May 22, 2025, including the portions of the Registrant’s proxy statement for the 2025 annual meeting of stockholders, filed with the SEC on June 13, 2025, incorporated by reference in Part III of the 2025 Annual Report on Form 10-K;

2.The Registrant’s Current Reports on Form 8-K filed with the SEC on June 5, 2025, July 29, 2025 and August 4, 2025 (but not any Item 2.02 or Exhibit 99.1 of such filing, which were furnished under applicable SEC rules rather than filed); and

3.The description of the Registrant’s capital stock filed as Exhibit 4.1 to its Annual Report on Form 10-K for the fiscal year ended March 31, 2025, filed with the SEC on May 22, 2025.


In addition, all documents filed by the Registrant with the SEC pursuant to Sections 13(a), 13(c), 14 and 15(d) of the Securities Exchange Act of 1934, as amended, subsequent to the date of this Registration Statement and prior to the filing of a post-effective amendment, which indicates that all securities offered have been sold or which deregisters all of such securities then remaining unsold, are deemed to be incorporated by reference in this Registration Statement and to be a part hereof from the respective dates of filing of such documents. Any statement contained in this Registration Statement or in a document incorporated by reference shall be deemed modified or superseded to the extent that a statement contained in any subsequently filed document which also is or is deemed to be incorporated by reference herein or therein modifies or supersedes such statement. Any statement so modified or superseded shall not be deemed to constitute a part hereof, except as so modified or superseded.

Item 8.    Exhibits.

Exhibit    Description                                            
5.1    Opinion of Skadden, Arps, Slate, Meagher & Flom LLP
10.1    8x8, Inc. Amended and Restated 2022 Equity Incentive Plan
10.2    8x8, Inc. Amended and Restated 1996 Employee Stock Purchase Plan
10.3    8x8, Inc. Amended and Restated 2017 New Employee Inducement Incentive Plan (incorporated by reference to Exhibit 10.1 to Form S-8 filed on February 5, 2025)
23.1    Consent of Skadden, Arps, Slate, Meagher and Flom (included in Exhibit 5.1)
23.2    Consent of Independent Registered Public Accounting Firm
24.1    Power of Attorney (included in signature page to this Registration Statement)
107    Calculation of Filing Fee Table
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SIGNATURES
Pursuant to the requirements of the Securities Act of 1933, as amended, the Registrant certifies that it has reasonable grounds to believe that it meets all of the requirements for filing on Form S-8 and has duly caused this Registration Statement to be signed on its behalf by the undersigned, thereunto duly authorized, in the city of Campbell, State of California, on the 4th day of August 2025.
8x8, Inc.
By: /s/ Samuel Wilson            
Samuel Wilson
Chief Executive Officer
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POWER OF ATTORNEY

KNOW ALL PERSONS BY THESE PRESENTS, that each person whose signature appears below hereby constitutes and appoints Samuel Wilson, Laurence Denny and Kevin Kraus, and each one of them, acting individually and without the other, as his or her true and lawful attorney-in-fact and agent, each with full power of substitution, for him and in his or her name, place and stead in any and all capacities, to sign any and all amendments to this Registration Statement (including post-effective amendments), and to file the same, with exhibits thereto and other documents in connection therewith, with the Securities and Exchange Commission, granting unto said attorneys-in-fact and agents, full power and authority to do and perform each and every act and thing requisite and necessary to be done, as fully to all intents and purposes as he or she might or could do in person, hereby ratifying and confirming all that each of said attorneys-in-fact or his substitute or substitutes may do or cause to be done by virtue hereof.

Pursuant to the requirements of the Securities Act of 1933, as amended, this Registration Statement has been signed by the following persons in the capacities and on the dates indicated.

 Signature
TitleDate
/s/ Samuel Wilson
Samuel Wilson
Chief Executive Officer and Director
(Principal Executive Officer and Director)
August 4, 2025
/s/ Kevin Kraus
Kevin Kraus
Chief Financial Officer
(Principal Financial Officer)
August 4, 2025
/s/ Jaswinder Pal Singh
Jaswinder Pal Singh
Chairman and DirectorAugust 4, 2025
/s/ Monique Bonner
Monique Bonner
Director August 4, 2025
/s/ Andrew Burton
Andrew Burton
DirectorAugust 4, 2025
/s/ Todd Ford
Todd Ford
DirectorAugust 4, 2025
/s/ Alison Gleeson
Alison Gleeson
DirectorAugust 4, 2025
/s/ John Pagliuca
John Pagliuca
DirectorAugust 4, 2025
/s/ Elizabeth Theophille
Elizabeth Theophille
DirectorAugust 4, 2025
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FAQ

What were Axsome Therapeutics' (AXSM) Q2 2025 revenues?

Net revenue totaled $150.0 million, up 72% from the prior-year quarter.

Did AXSM reduce its net loss in Q2 2025?

Yes. Net loss improved to $48.0 million (�$0.97/sh) from $79.3 million (�$1.67/sh) a year ago.

How much cash does Axsome have and how long will it last?

Cash & equivalents were $303 million on 30 Jun 2025; management projects funding for at least the next 12 months.

What are the key terms of the May 2025 Blackstone loan agreement?

Up to $570 million: $120 M term loan drawn, $180 M delayed-draw, $70 M revolver (drawn), SOFR+4.75%/4.00% rates, five-year maturity.

When was Symbravo approved and launched?

Symbravo received FDA approval in January 2025 and became commercially available in the U.S. in June 2025.

How many AXSM shares were outstanding?

There were 49,901,487 common shares outstanding as of 28 Jul 2025.

What is Axsome's current debt level?

Long-term loan payable is $117.5 million with an additional $70 million revolver classified as short-term.
8X8 Inc

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Software - Application
Services-computer Processing & Data Preparation
United States
CAMPBELL