X4 Pharmaceuticals Announces Pricing of $135 Million Underwritten Public Offering
X4 Pharmaceuticals (Nasdaq: XFOR) priced an underwritten public offering of 45,860,000 shares at $2.90 per share and up to 700,000 pre-funded warrants at $2.899 each (exercise price $0.001). The offering is expected to generate approximately $135 million in gross proceeds before underwriting discounts, commissions and expenses and is expected to close on October 27, 2025, subject to customary conditions.
X4 granted underwriters a 30-day option to buy up to an additional 6,984,000 shares. Net proceeds will fund the pivotal Phase 3 development of mavorixafor in certain chronic neutropenic disorders and support general corporate purposes.
X4 Pharmaceuticals (Nasdaq: XFOR) ha fissato un'offerta pubblica sottoscritta garantita da 45.860.000 azioni a $2,90 per azione e fino a 700.000 warrant prefinanziati a $2,899 ciascuno (prezzo di esercizio $0,001). L'offerta dovrebbe generare circa $135 milioni di proventi lordi prima delle commissioni, degli sconti e delle spese di collocamento e dovrebbe chiudersi il 27 ottobre 2025, soggetta alle condizioni usuali.
X4 ha concesso agli underwriter un'opzione di 30 giorni per acquistare fino a un ulteriore 6.984.000 azioni. I proventi netti serviranno a finanziare lo sviluppo di fase 3 di mavorixafor in alcuni disturbi neutropenici cronici e a supportare fini aziendali generali.
X4 Pharmaceuticals (Nasdaq: XFOR) fijó una oferta pública suscrita nominal, de 45,860,000 acciones a $2.90 por acción y hasta 700,000 warrants prefinanciados a $2.899 cada uno (precio de ejercicio $0.001). Se espera que la oferta genere aproximadamente $135 millones en ingresos brutos antes de descuentos, comisiones y gastos y se espera que cierre el 27 de octubre de 2025, sujeto a condiciones habituales.
X4 otorgó a los suscriptores una opción de 30 días para comprar hasta 6,984,000 acciones adicionales. Los ingresos netos financiarán el desarrollo de la Fase 3 de mavorixafor en ciertos trastornos neutropénicos crónicos y apoyarán fines corporativos generales.
X4 Pharmaceuticals (Nasdaq: XFOR) 은 45,860,000 주의 공모 주식과 대당 $2.90의 가격으로, 그리고 최대 700,000 사전 발행 워런트를 $2.899에 각각 발행하여 언더라이팅 공모를 가격 결정했습니다 (행사가 $0.001). 이 공모는 약 $135 million의 총수익을 예상하며, 언더라이팅 할인, 커미션 및 비용을 차감하기 전의 금액이며, 2025년 10월 27일에 마감될 예정이며 일반적인 조건에 따라 마감될 수 있습니다.
X4는 주관사들에게 추가로 6,984,000 주를 30일 옵션으로 매입할 수 있는 권한을 부여했습니다. 순수익은 mavorixafor의 3상 개발을 특정 만성 중성구성 장애에 대해 진행하는 데 자금을 지원하고 일반 기업 용도로도 사용될 것입니다.
X4 Pharmaceuticals (Nasdaq: XFOR) a fixé une offre publique souscrite et garantie par les teneurs de livre de 45 860 000 actions à $2,90 par action et jusqu'à 700 000 warrants préfinancés à $2,899 chacun (prix d'exercice 0,001 $). L'offre devrait générer environ $135 millions de produits bruts avant remises, commissions et frais et devrait être clôturée le 27 octobre 2025, sous réserve des conditions habituelles.
X4 a accordé aux souscripteurs une option de 30 jours pour acheter jusqu'à 6 984 000 actions supplémentaires. Le produit net servira à financer le développement pivot de la Phase 3 de mavorixafor dans certaines affections neutropéniques chroniques et à soutenir des fins générales de l'entreprise.
X4 Pharmaceuticals (Nasdaq: XFOR) hat eine unterzeichnete öffentliche Offerte von 45.860.000 Aktien zu $2,90 pro Aktie und bis zu 700.000 vorfinanzierte Warrants zu $2,899 je angeboten (Ausübungspreis $0,001). Die Offerte wird voraussichtlich ca. $135 Millionen Bruttoerlöse vor Underwriting-Abschlägen, Provisionen und Kosten generieren und voraussichtlich am 27. Oktober 2025 abgeschlossen, vorbehaltlich üblicher Bedingungen.
X4 hat den Underwritern eine 30-tägige Option eingeräumt, bis zu zusätzlich 6.984.000 Aktien zu erwerben. Die Nettobeträge dienen der Finanzierung der entscheidenden Phase-3-Entwicklung von mavorixafor bei bestimmten chronischen neutropenischen Erkrankungen und unterstützen allgemeine Unternehmenszwecke.
X4 Pharmaceuticals (الشركة المدرجة في Nasdaq: XFOR) حددت عرضاً عاماً اكتتابياً مدعوماً من قبل الماجرِّين بقيمة 45,860,000 سهماً بسعر $2.90 للسهم الواحد وبحد أقصى 700,000 وورنت مدفوعة مسبقاً بسعر $2.899 لكل واحد (سعر الممارسة $0.001). من المتوقع أن يولّد العرض نحو $135 مليون من العوائد الإجمالية قبل خصومات الاكتتاب والعمولات والنفقات، ومن المتوقع أن يغلق في 27 أكتوبر 2025، رهناً بالشروط المعتادة.
منحت X4 للمكتتبين خياراً لمدة 30 يوماً لشراء حتى 6,984,000 سهم إضافي. ستُستخدم العائدات الصافيه لتمويل التطوير الحاسم للمرحلة 3 من mavorixafor في بعض الاضطرابات neutropenic المزمنة ولدعم أغراض الشركة العامة.
X4 Pharmaceuticals (纳斯达克: XFOR) 已定价一项承销的公开发行,发行45,860,000 股,每股价格为 $2.90,以及最多 700,000 预先资金认股权证,每个价格为 $2.899(行权价 $0.001)。该发行在承销折扣、佣金和费用之前,预计将产生约 $135 百万美元的毛收入,预计将于 2025 年 10 月 27 日完成,需符合惯常条件。
X4 授予承销商一个30天的期权,以购买额外的 6,984,000 股。净收益将用于资助 mavorixafor 在某些慢性中性粒细胞减少症中的关键第三阶段开发,并支持公司的通用企业用途。
- Expected gross proceeds of approximately $135 million
- Proceeds earmarked to fund pivotal Phase 3 mavorixafor development
- Underwriters engaged: Leerink, Stifel, Guggenheim
- Offering includes 45.86M new shares, causing shareholder dilution
- Underwriters hold a 30-day option for 6.984M additional shares
- Pre-funded warrants exercisable immediately, increasing near-term dilution
Insights
Equity raise secures funding for a pivotal Phase 3 program and near-term operations.
X4 Pharmaceuticals priced an underwritten offering to raise approximately
The transaction directly funds the pivotal Phase 3 development of mavorixafor in certain chronic neutropenic disorders and replenishes working capital. The size and immediate exercisability of the pre-funded warrants reduce exercise timing risk and provide near-term liquidity, while underwriter options create optional incremental dilution risk if exercised.
Key dependencies include successful closing on
BOSTON, Oct. 24, 2025 (GLOBE NEWSWIRE) -- X4 Pharmaceuticals (Nasdaq: XFOR) (“X4” or the “Company”), a company driven to improve the lives of people with rare hematology diseases, today announced the pricing of its previously announced underwritten public offering of 45,860,000 shares of its common stock at a public offering price per share of
X4 intends to use the net proceeds from this offering, together with its existing cash and cash equivalents and cash flows from operations, to fund the pivotal Phase 3 development of mavorixafor in certain chronic neutropenic disorders, as well as for general and administrative expenses, capital expenditures, working capital and other general corporate purposes.
Leerink Partners, Stifel and Guggenheim Securities are acting as joint bookrunning managers for the proposed offering.
A shelf registration statement relating to these securities was filed with the Securities and Exchange Commission (SEC) on August 14, 2023 and became effective on August 24, 2023. This offering is being made only by means of a written prospectus, including a prospectus supplement, forming a part of the effective registration statement. A preliminary prospectus supplement and accompanying prospectus relating to the offering have been filed with the SEC and are available on the SEC’s website, located at www.sec.gov. A copy of the final prospectus supplement and the accompanying prospectus relating to the offering will be filed with the SEC and will be available on the SEC’s website at www.sec.gov and, when available, may be obtained from: Leerink Partners LLC, Syndicate Department, 53 State Street, 40th Floor, Boston, Massachusetts 02109, by telephone at (800) 808-7525 ext. 6105, or by emailing syndicate@leerink.com; Stifel, Nicolaus & Company, Incorporated, Attention: Prospectus Department, One Montgomery Street, Suite 3700, San Francisco, California 94104, by telephone at (415) 364-2720 or by emailing syndprospectus@stifel.com; or Guggenheim Securities, LLC at 330 Madison Avenue, 8th Floor, New York, NY 10017, Attention: Equity Syndicate Department, by telephone at (212) 518-9544, or by email at GSEquityProspectusDelivery@guggenheimpartners.com.
This press release shall not constitute an offer to sell, or the solicitation of an offer to buy, nor shall there be any sale of these securities in any state or jurisdiction in which such offer, solicitation, or sale would be unlawful prior to registration or qualification under the securities laws of any such state or jurisdiction.
About X4 Pharmaceuticals
X4 is delivering progress for patients by developing and commercializing innovative therapies for those with rare hematology diseases and significant unmet needs. Leveraging expertise in CXCR4, X4 has successfully developed mavorixafor, an orally available CXCR4 antagonist that is currently being marketed in the U.S. as XOLREMDI® in its first indication. The Company is also evaluating additional uses of mavorixafor and is conducting a global, pivotal Phase 3 clinical trial (4WARD) in people with certain chronic neutropenic disorders. X4 is headquartered in Boston, Massachusetts.
X4 Forward-Looking Statements
This press release contains forward-looking statements within the meaning of applicable securities laws, including the Private Securities Litigation Reform Act of 1995, as amended. These statements may be identified by the words “may,” “will,” “could,” “would,” “should,” “expect,” “plan,” “anticipate,” “intend,” “believe,” “estimate,” “predict,” “project,” “potential,” “continue,” “target,” or other similar terms or expressions that concern X4’s expectations, strategy, business, plans, or intentions. Forward-looking statements include, without limitation, implied or express statements regarding: X4’s expectations regarding the consummation of the offering, the anticipated use of proceeds from the offering, the satisfaction of customary closing conditions with respect to the offering and the potential value and clinical benefit of the Company’s product candidates. Any forward-looking statements in this press release are based on management’s current expectations and beliefs. These forward-looking statements are neither promises nor guarantees of future performance, and are subject to a variety of risks and uncertainties, many of which are beyond X4’s control, which could cause actual results to differ materially from those contemplated in these forward-looking statements, including the risks that: X4 may be unable to advance and commercialize mavorixafor to treat chronic neutropenia or to gain ex-U.S. approval for the treatment of WHIM; the expected sufficiency of X4’s existing cash resources and runway may not be accurate; the expected availability, content, and timing of clinical data from X4’s ongoing clinical trials of mavorixafor may be delayed or unavailable, including the ongoing Phase 3 clinical trial in chronic neutropenia; trials, studies and research programs may not have satisfactory outcomes; earlier trials and studies may not be predictive of later trials and studies; the design and rate of enrollment for clinical trials, including the ongoing Phase 3 clinical trial evaluating mavorixafor in certain chronic neutropenic disorders may not enable successful completion of the trial(s); the commercial opportunity for mavorixafor in chronic neutropenic disorders may be smaller than anticipated; X4 may be unable to obtain and maintain regulatory approvals; adverse safety effects may arise from the testing or use of the Company’s product and product candidates; and other risks and uncertainties, including those described in the section entitled “Risk Factors” in X4’s most recent Annual Report on Form 10-K filed with the SEC and in subsequent filings X4 makes with the SEC from time to time. X4 undertakes no obligation to update the information contained in this presentation to reflect new events or circumstances, except as required by law.
X4 Investor Contact:
IR@X4pharma.com