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[8-K] ServisFirst Bancshares Inc. Reports Material Event

Filing Impact
(Moderate)
Filing Sentiment
(Neutral)
Form Type
8-K
Rhea-AI Filing Summary

Medicus Pharma Ltd. (Nasdaq: MDCX) has entered into a definitive agreement to acquire 100% of Antev Limited, a private clinical-stage biotech developing Teverelix, a next-generation GnRH antagonist for high-risk prostate cancer and acute urinary retention.

Consideration: Medicus will issue 2,666,600 common shares—about 17% of its outstanding stock—as upfront payment ("Consideration Shares").

Lock-up & Governance: Consideration Shares are subject to a staggered lock-up for up to 36 months and a voting agreement favoring current MDCX management.

Earn-out: Antev shareholders may receive up to US$65 million in additional contingent consideration tied to future FDA Phase 2 and NDA milestones.

Closing timeline: Targeted before end-August 2025, pending Antev shareholder, regulatory and other customary approvals; no guarantee of completion.

Registration statement context: The prospectus supplement registers up to 3.71 million MDCX shares and incorporates the accompanying Form 8-K detailing the Antev deal.

Market data: MDCX last traded at $2.90 on 27 June 2025; the company qualifies as an emerging growth company with scaled disclosure.

Investment view: The transaction broadens Medicus’s pipeline and aligns payment with clinical success, but introduces ~17% dilution and execution risk on an early-stage asset.

Medicus Pharma Ltd. (Nasdaq: MDCX) ha stipulato un accordo definitivo per acquisire il 100% di Antev Limited, una biotech privata in fase clinica che sviluppa Teverelix, un antagonista GnRH di nuova generazione per il cancro alla prostata ad alto rischio e il ritenzione urinaria acuta.

Considerazione: Medicus emetterà 2.666.600 azioni ordinarie — circa il 17% del capitale sociale in circolazione — come pagamento anticipato ("Azioni di Considerazione").

Vincoli e governance: Le Azioni di Considerazione saranno soggette a un lock-up scaglionato fino a 36 mesi e a un accordo di voto a favore dell’attuale management di MDCX.

Earn-out: Gli azionisti di Antev potranno ricevere fino a 65 milioni di dollari USA in ulteriori compensi condizionati legati ai futuri traguardi FDA di Fase 2 e NDA.

Tempistica di chiusura: Prevista entro fine agosto 2025, subordinata all’approvazione degli azionisti di Antev, delle autorità di regolamentazione e ad altri consueti permessi; nessuna garanzia di completamento.

Contesto della dichiarazione di registrazione: Il supplemento al prospetto registra fino a 3,71 milioni di azioni MDCX e incorpora il modulo 8-K allegato che dettaglia l’accordo con Antev.

Dati di mercato: MDCX ha chiuso a 2,90 $ il 27 giugno 2025; la società è qualificata come emerging growth company con disclosure semplificata.

Opinione sull’investimento: L’operazione amplia il portafoglio di Medicus e allinea il pagamento al successo clinico, ma comporta una diluizione di circa il 17% e un rischio di esecuzione su un asset in fase precoce.

Medicus Pharma Ltd. (Nasdaq: MDCX) ha firmado un acuerdo definitivo para adquirir el 100% de Antev Limited, una biotecnológica privada en fase clínica que desarrolla Teverelix, un antagonista GnRH de próxima generación para el cáncer de próstata de alto riesgo y la retención urinaria aguda.

Consideración: Medicus emitirá 2.666.600 acciones comunes — alrededor del 17% de sus acciones en circulación — como pago inicial ("Acciones de Consideración").

Bloqueo y gobernanza: Las Acciones de Consideración estarán sujetas a un bloqueo escalonado de hasta 36 meses y a un acuerdo de voto que favorece a la actual dirección de MDCX.

Earn-out: Los accionistas de Antev podrían recibir hasta 65 millones de dólares estadounidenses adicionales en contraprestaciones contingentes vinculadas a futuros hitos de FDA en Fase 2 y NDA.

Plazo de cierre: Previsto antes de finales de agosto de 2025, sujeto a la aprobación de los accionistas de Antev, reguladores y otras aprobaciones habituales; sin garantía de finalización.

Contexto de la declaración de registro: El suplemento al prospecto registra hasta 3,71 millones de acciones MDCX e incorpora el Formulario 8-K adjunto que detalla el acuerdo con Antev.

Datos de mercado: MDCX cotizó por última vez a 2,90 $ el 27 de junio de 2025; la compañía califica como empresa emergente con divulgación escalada.

Perspectiva de inversión: La transacción amplía la cartera de Medicus y alinea el pago con el éxito clínico, pero introduce una dilución de aproximadamente el 17% y riesgo de ejecución sobre un activo en etapa temprana.

Medicus Pharma Ltd. (나스닥: MDCX)는 고위험 전립선암 및 급성 요정체 치료를 위한 차세대 GnRH 길항제인 Teverelix를 개발하는 임상 단계 비공개 바이오텍 Antev Limited의 100% 인수를 위한 최종 계약을 체결했습니다.

대가: Medicus는 선급금으로서 약 17%의 발행 주식에 해당하는 2,666,600주의 보통주(“대가 주식”)를 발행할 예정입니다.

락업 및 거버넌스: 대가 주식은 최대 36개월에 걸친 단계적 락업과 현재 MDCX 경영진에 유리한 의결권 계약의 적용을 받습니다.

성과기반 지급(Earn-out): Antev 주주들은 FDA 2상 및 NDA 향후 마일스톤 달성에 따라 최대 6,500만 달러의 추가 조건부 대가를 받을 수 있습니다.

종료 일정: Antev 주주, 규제 당국 및 기타 통상 승인 완료를 조건으로 2025년 8월 말 이전 완료를 목표로 하며, 완료 보장은 없습니다.

등록 서류 관련: 증권 설명서 보충서에는 최대 371만주의 MDCX 주식 등록이 포함되며, Antev 거래 내용을 상세히 담은 Form 8-K가 포함되어 있습니다.

시장 데이터: MDCX는 2025년 6월 27일 종가 기준 2.90달러에 거래되었으며, 신생 성장 기업으로서 간소화된 공시 요건을 충족합니다.

투자 의견: 이번 거래는 Medicus의 파이프라인을 확장하고 임상 성공에 따른 지급 구조를 갖추었으나, 약 17%의 희석 효과와 초기 단계 자산에 대한 실행 위험이 존재합니다.

Medicus Pharma Ltd. (Nasdaq : MDCX) a conclu un accord définitif pour acquérir 100 % d’Antev Limited, une biotech privée en phase clinique développant Teverelix, un antagoniste de la GnRH de nouvelle génération destiné au cancer de la prostate à haut risque et à la rétention urinaire aiguë.

Contrepartie : Medicus émettra 2 666 600 actions ordinaires — soit environ 17 % de son capital en circulation — en paiement initial (« Actions de Contrepartie »).

Blocage et gouvernance : Les Actions de Contrepartie seront soumises à un blocage échelonné pouvant aller jusqu’à 36 mois, ainsi qu’à un accord de vote favorisant la direction actuelle de MDCX.

Earn-out : Les actionnaires d’Antev pourront recevoir jusqu’à 65 millions de dollars US supplémentaires en contrepartie conditionnelle liée aux futurs jalons FDA de phase 2 et de NDA.

Calendrier de clôture : Prévu avant fin août 2025, sous réserve de l’approbation des actionnaires d’Antev, des autorités réglementaires et d’autres approbations habituelles ; aucune garantie de réalisation.

Contexte de la déclaration d’enregistrement : Le supplément au prospectus enregistre jusqu’à 3,71 millions d’actions MDCX et intègre le formulaire 8-K joint détaillant l’accord avec Antev.

Données de marché : MDCX a clôturé à 2,90 $ le 27 juin 2025 ; la société est qualifiée d’entreprise en forte croissance avec des obligations de divulgation allégées.

Opinion d’investissement : La transaction élargit le portefeuille de Medicus et aligne le paiement sur le succès clinique, mais entraîne une dilution d’environ 17 % ainsi qu’un risque d’exécution lié à un actif en phase précoce.

Medicus Pharma Ltd. (Nasdaq: MDCX) hat eine endgültige Vereinbarung zum Erwerb von 100 % von Antev Limited getroffen, einem privaten Biotech-Unternehmen in der klinischen Entwicklungsphase, das Teverelix entwickelt, einen neuartigen GnRH-Antagonisten für Hochrisiko-Prostatakrebs und akuten Harnverhalt.

Vergütung: Medicus wird 2.666.600 Stammaktien ausgeben – etwa 17 % der ausstehenden Aktien – als Vorauszahlung ("Vergütungsaktien").

Lock-up & Governance: Die Vergütungsaktien unterliegen einem gestaffelten Lock-up von bis zu 36 Monaten sowie einer Stimmrechtsvereinbarung zugunsten des aktuellen MDCX-Managements.

Earn-out: Antev-Aktionäre können bis zu 65 Millionen US-Dollar an zusätzlicher erfolgsabhängiger Vergütung erhalten, die an zukünftige FDA-Phase-2- und NDA-Meilensteine gebunden ist.

Abschlusszeitplan: Geplant vor Ende August 2025, vorbehaltlich der Zustimmung der Antev-Aktionäre, regulatorischer und sonstiger üblicher Genehmigungen; kein Abschluss garantiert.

Kontext der Registrierungserklärung: Das Prospektergänzungsblatt registriert bis zu 3,71 Millionen MDCX-Aktien und enthält das beigefügte Formular 8-K, das das Antev-Geschäft detailliert.

Marktdaten: MDCX wurde zuletzt am 27. Juni 2025 zu 2,90 $ gehandelt; das Unternehmen qualifiziert sich als Emerging Growth Company mit reduzierten Offenlegungspflichten.

Investmentmeinung: Die Transaktion erweitert die Pipeline von Medicus und koppelt die Zahlung an den klinischen Erfolg, führt jedoch zu einer Verwässerung von etwa 17 % und birgt Ausführungsrisiken bei einem Asset in einem frühen Entwicklungsstadium.

Positive
  • Pipeline expansion: Acquisition brings Teverelix, a novel GnRH antagonist targeting prostate cancer and AURr, adding growth optionality to MDCX.
  • Cash conservation: All-share consideration preserves balance-sheet liquidity for future R&D needs.
  • Aligned incentives: Up to US$65 M milestone payments are contingent on FDA successes, limiting upfront value transfer.
  • Lock-up provisions: 36-month staggered restrictions reduce immediate selling pressure from Antev shareholders.
Negative
  • Share dilution: Issuance of 2.67 M shares increases basic share count by ~17%, potentially weighing on per-share metrics.
  • Clinical risk: Teverelix is only at the Phase 2 threshold, carrying high failure probability.
  • Contingent liabilities: Earn-outs of up to US$65 M could strain resources if milestones are achieved without commensurate cash inflow.
  • Deal uncertainty: Closing subject to multiple approvals; failure would nullify expected strategic benefits.

Insights

TL;DR: Stock-for-stock acquisition adds pipeline upside but brings 17% dilution and milestone liabilities—net neutral/lean positive near term.

The all-share structure conserves cash but increases dilution; 2.67 M new shares compare to ~15.5 M basic shares (~17%). Lock-ups reduce immediate selling pressure, mitigating technical overhang. The US$65 M milestone, while sizable, is success-based and therefore non–cash until value-creating events occur. Absent revenue or late-stage data, valuation hinges on Teverelix’s clinical outlook, which remains Phase-2 dependent. Closing risk persists (shareholder and regulatory approvals), so near-term impact is contingent. Overall, modestly constructive for long-term growth, neutral for short-term fundamentals.

TL;DR: Deal gives MDCX a differentiated GnRH antagonist with niche cardio-safety angle—strategic but still high clinical risk.

Teverelix targets cardiovascular-high-risk prostate cancer patients, an underserved segment where next-gen antagonists could command premium pricing. If efficacy/safety profile holds, first-in-class positioning could unlock substantial market share. However, asset is only entering U.S. Phase 2; historical success rate from Phase 2 to approval in urology/oncology is ~10-15%. Earn-out aligns costs with progress, but potential US$65 M liability would hit just as commercial investment ramps. From a sector standpoint, transaction is a typical platform-expansion play with speculative upside; impact rated neutral until clinical data de-risks.

Medicus Pharma Ltd. (Nasdaq: MDCX) ha stipulato un accordo definitivo per acquisire il 100% di Antev Limited, una biotech privata in fase clinica che sviluppa Teverelix, un antagonista GnRH di nuova generazione per il cancro alla prostata ad alto rischio e il ritenzione urinaria acuta.

Considerazione: Medicus emetterà 2.666.600 azioni ordinarie — circa il 17% del capitale sociale in circolazione — come pagamento anticipato ("Azioni di Considerazione").

Vincoli e governance: Le Azioni di Considerazione saranno soggette a un lock-up scaglionato fino a 36 mesi e a un accordo di voto a favore dell’attuale management di MDCX.

Earn-out: Gli azionisti di Antev potranno ricevere fino a 65 milioni di dollari USA in ulteriori compensi condizionati legati ai futuri traguardi FDA di Fase 2 e NDA.

Tempistica di chiusura: Prevista entro fine agosto 2025, subordinata all’approvazione degli azionisti di Antev, delle autorità di regolamentazione e ad altri consueti permessi; nessuna garanzia di completamento.

Contesto della dichiarazione di registrazione: Il supplemento al prospetto registra fino a 3,71 milioni di azioni MDCX e incorpora il modulo 8-K allegato che dettaglia l’accordo con Antev.

Dati di mercato: MDCX ha chiuso a 2,90 $ il 27 giugno 2025; la società è qualificata come emerging growth company con disclosure semplificata.

Opinione sull’investimento: L’operazione amplia il portafoglio di Medicus e allinea il pagamento al successo clinico, ma comporta una diluizione di circa il 17% e un rischio di esecuzione su un asset in fase precoce.

Medicus Pharma Ltd. (Nasdaq: MDCX) ha firmado un acuerdo definitivo para adquirir el 100% de Antev Limited, una biotecnológica privada en fase clínica que desarrolla Teverelix, un antagonista GnRH de próxima generación para el cáncer de próstata de alto riesgo y la retención urinaria aguda.

Consideración: Medicus emitirá 2.666.600 acciones comunes — alrededor del 17% de sus acciones en circulación — como pago inicial ("Acciones de Consideración").

Bloqueo y gobernanza: Las Acciones de Consideración estarán sujetas a un bloqueo escalonado de hasta 36 meses y a un acuerdo de voto que favorece a la actual dirección de MDCX.

Earn-out: Los accionistas de Antev podrían recibir hasta 65 millones de dólares estadounidenses adicionales en contraprestaciones contingentes vinculadas a futuros hitos de FDA en Fase 2 y NDA.

Plazo de cierre: Previsto antes de finales de agosto de 2025, sujeto a la aprobación de los accionistas de Antev, reguladores y otras aprobaciones habituales; sin garantía de finalización.

Contexto de la declaración de registro: El suplemento al prospecto registra hasta 3,71 millones de acciones MDCX e incorpora el Formulario 8-K adjunto que detalla el acuerdo con Antev.

Datos de mercado: MDCX cotizó por última vez a 2,90 $ el 27 de junio de 2025; la compañía califica como empresa emergente con divulgación escalada.

Perspectiva de inversión: La transacción amplía la cartera de Medicus y alinea el pago con el éxito clínico, pero introduce una dilución de aproximadamente el 17% y riesgo de ejecución sobre un activo en etapa temprana.

Medicus Pharma Ltd. (나스닥: MDCX)는 고위험 전립선암 및 급성 요정체 치료를 위한 차세대 GnRH 길항제인 Teverelix를 개발하는 임상 단계 비공개 바이오텍 Antev Limited의 100% 인수를 위한 최종 계약을 체결했습니다.

대가: Medicus는 선급금으로서 약 17%의 발행 주식에 해당하는 2,666,600주의 보통주(“대가 주식”)를 발행할 예정입니다.

락업 및 거버넌스: 대가 주식은 최대 36개월에 걸친 단계적 락업과 현재 MDCX 경영진에 유리한 의결권 계약의 적용을 받습니다.

성과기반 지급(Earn-out): Antev 주주들은 FDA 2상 및 NDA 향후 마일스톤 달성에 따라 최대 6,500만 달러의 추가 조건부 대가를 받을 수 있습니다.

종료 일정: Antev 주주, 규제 당국 및 기타 통상 승인 완료를 조건으로 2025년 8월 말 이전 완료를 목표로 하며, 완료 보장은 없습니다.

등록 서류 관련: 증권 설명서 보충서에는 최대 371만주의 MDCX 주식 등록이 포함되며, Antev 거래 내용을 상세히 담은 Form 8-K가 포함되어 있습니다.

시장 데이터: MDCX는 2025년 6월 27일 종가 기준 2.90달러에 거래되었으며, 신생 성장 기업으로서 간소화된 공시 요건을 충족합니다.

투자 의견: 이번 거래는 Medicus의 파이프라인을 확장하고 임상 성공에 따른 지급 구조를 갖추었으나, 약 17%의 희석 효과와 초기 단계 자산에 대한 실행 위험이 존재합니다.

Medicus Pharma Ltd. (Nasdaq : MDCX) a conclu un accord définitif pour acquérir 100 % d’Antev Limited, une biotech privée en phase clinique développant Teverelix, un antagoniste de la GnRH de nouvelle génération destiné au cancer de la prostate à haut risque et à la rétention urinaire aiguë.

Contrepartie : Medicus émettra 2 666 600 actions ordinaires — soit environ 17 % de son capital en circulation — en paiement initial (« Actions de Contrepartie »).

Blocage et gouvernance : Les Actions de Contrepartie seront soumises à un blocage échelonné pouvant aller jusqu’à 36 mois, ainsi qu’à un accord de vote favorisant la direction actuelle de MDCX.

Earn-out : Les actionnaires d’Antev pourront recevoir jusqu’à 65 millions de dollars US supplémentaires en contrepartie conditionnelle liée aux futurs jalons FDA de phase 2 et de NDA.

Calendrier de clôture : Prévu avant fin août 2025, sous réserve de l’approbation des actionnaires d’Antev, des autorités réglementaires et d’autres approbations habituelles ; aucune garantie de réalisation.

Contexte de la déclaration d’enregistrement : Le supplément au prospectus enregistre jusqu’à 3,71 millions d’actions MDCX et intègre le formulaire 8-K joint détaillant l’accord avec Antev.

Données de marché : MDCX a clôturé à 2,90 $ le 27 juin 2025 ; la société est qualifiée d’entreprise en forte croissance avec des obligations de divulgation allégées.

Opinion d’investissement : La transaction élargit le portefeuille de Medicus et aligne le paiement sur le succès clinique, mais entraîne une dilution d’environ 17 % ainsi qu’un risque d’exécution lié à un actif en phase précoce.

Medicus Pharma Ltd. (Nasdaq: MDCX) hat eine endgültige Vereinbarung zum Erwerb von 100 % von Antev Limited getroffen, einem privaten Biotech-Unternehmen in der klinischen Entwicklungsphase, das Teverelix entwickelt, einen neuartigen GnRH-Antagonisten für Hochrisiko-Prostatakrebs und akuten Harnverhalt.

Vergütung: Medicus wird 2.666.600 Stammaktien ausgeben – etwa 17 % der ausstehenden Aktien – als Vorauszahlung ("Vergütungsaktien").

Lock-up & Governance: Die Vergütungsaktien unterliegen einem gestaffelten Lock-up von bis zu 36 Monaten sowie einer Stimmrechtsvereinbarung zugunsten des aktuellen MDCX-Managements.

Earn-out: Antev-Aktionäre können bis zu 65 Millionen US-Dollar an zusätzlicher erfolgsabhängiger Vergütung erhalten, die an zukünftige FDA-Phase-2- und NDA-Meilensteine gebunden ist.

Abschlusszeitplan: Geplant vor Ende August 2025, vorbehaltlich der Zustimmung der Antev-Aktionäre, regulatorischer und sonstiger üblicher Genehmigungen; kein Abschluss garantiert.

Kontext der Registrierungserklärung: Das Prospektergänzungsblatt registriert bis zu 3,71 Millionen MDCX-Aktien und enthält das beigefügte Formular 8-K, das das Antev-Geschäft detailliert.

Marktdaten: MDCX wurde zuletzt am 27. Juni 2025 zu 2,90 $ gehandelt; das Unternehmen qualifiziert sich als Emerging Growth Company mit reduzierten Offenlegungspflichten.

Investmentmeinung: Die Transaktion erweitert die Pipeline von Medicus und koppelt die Zahlung an den klinischen Erfolg, führt jedoch zu einer Verwässerung von etwa 17 % und birgt Ausführungsrisiken bei einem Asset in einem frühen Entwicklungsstadium.

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UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

_________________

FORM 8-K

_________________

CURRENT REPORT

Pursuant to Section 13 or 15(d)
of the Securities Exchange Act of 1934

Date of Report (Date of earliest event reported):  June 16, 2025

_______________________________

ServisFirst Bancshares, Inc.

(Exact name of registrant as specified in its charter)

_______________________________

Delaware001-3645226-0734029
(State or Other Jurisdiction of Incorporation)(Commission File Number)(I.R.S. Employer Identification No.)

2500 Woodcrest Place

Birmingham, Alabama 35209

(Address of Principal Executive Offices) (Zip Code)

(205) 949-0302

(Registrant's telephone number, including area code)

Not Applicable

(Former name or former address, if changed since last report)

_______________________________

Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:

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 Symbol(s)Name of each exchange on which registered
CommonSFBSNew York Stock Exchange

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 8.01. Other Events.

 

On June 17, 2025, ServisFirst Bancshares, Inc. (“ServisFirst”) announced that the Board of Directors declared a quarterly cash dividend of $0.335 per share, payable on July 9, 2025 to stockholders of record as of July 1, 2025. A copy of the press release is attached hereto as Exhibit 99.1 and is incorporated herein by reference.

 

Item 9.01. Financial Statements and Exhibits.

 

(a)                 Not applicable

(b)                 Not applicable

(c)                 Not applicable

(d)                 Exhibits. The following exhibits are included with this Current Report on Form 8-K:

 

Exhibit No. Description
   
99.1 Press Release dated June 17, 2025.
104 Cover Page Interactive Data File (embedded within the Inline XBRL document)
 
 

 

SIGNATURE

 

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

 

 ServisFirst Bancshares, Inc.
   
  
Date: June 30, 2025By: /s/ Thomas A. Broughton, III        
  Thomas A. Broughton, III
  Chairman, President and Chief Executive Officer
  

 

FAQ

What did Medicus Pharma (MDCX) announce on June 30 2025?

The company entered a definitive agreement to acquire Antev Limited in an all-share deal worth 2.67 M MDCX shares plus up to US$65 M in milestones.

How much dilution will the Antev acquisition cause for MDCX shareholders?

Approximately 17% of the post-deal share count will be issued to Antev shareholders as Consideration Shares.

When is the Medicus–Antev transaction expected to close?

Management targets closure before the end of August 2025, subject to shareholder and regulatory approvals.

What milestones trigger the additional US$65 million payment to Antev shareholders?

Payments are tied to successful U.S. FDA Phase 2 completion and eventual New Drug Application approval for Teverelix.

Is there a lock-up on the new shares issued to Antev holders?

Yes, the 2.67 M Consideration Shares are subject to a staggered lock-up and voting agreement for up to 36 months.

What is Teverelix and why is it significant?

Teverelix is a next-gen GnRH antagonist targeting high-risk prostate cancer and AURr; it could be first-to-market in this niche if successful.
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