Acrivon Therapeutics Announces Inducement Grant Under Nasdaq Listing Rule 5635(c)(4)
Acrivon Therapeutics (Nasdaq: ACRV), a clinical stage precision medicine company, announced the approval of equity awards under its 2023 Inducement Plan for certain employees. The awards, granted on October 15, 2024, consist of stock options to purchase a total of 61,950 shares of Acrivon common stock.
The stock options will vest according to the following schedule:
- 25% on the first anniversary of the first day of the month following each employee's effective employment date
- Additional 2.083% installments monthly thereafter
Vesting is subject to continued employment. The inducement grants were approved by Acrivon's Board of Directors in compliance with Nasdaq Rule 5635(c)(4) and serve as a material inducement to employment.
Acrivon Therapeutics (Nasdaq: ACRV), un'azienda di medicina di precisione in fase clinica, ha annunciato l'approvazione di premi azionari nell'ambito del suo Piano di Induzione 2023 per determinati dipendenti. I premi, concessi il 15 ottobre 2024, consistono in opzioni di acquisto per un totale di 61.950 azioni della comune azionariato di Acrivon.
Le opzioni saranno maturate secondo il seguente programma:
- 25% nel primo anniversario del primo giorno del mese successivo alla data di assunzione effettiva di ciascun dipendente
- Ulteriori rate mensili del 2,083% successivamente
La maturazione è soggetta a un impiego continuativo. I premi di indennità sono stati approvati dal Consiglio di Amministrazione di Acrivon in conformità con la Regola Nasdaq 5635(c)(4) e fungono da incentivo materiale per l'impiego.
Acrivon Therapeutics (Nasdaq: ACRV), una empresa de medicina de precisión en etapa clínica, anunció la aprobación de premios de equidad bajo su Plan de Inducción 2023 para ciertos empleados. Los premios, otorgados el 15 de octubre de 2024, consisten en opciones de acciones para comprar un total de 61,950 acciones de la acción común de Acrivon.
Las opciones de acciones se consolidarán según el siguiente cronograma:
- 25% en el primer aniversario del primer día del mes siguiente a la fecha efectiva de empleo de cada empleado
- Instalaciones adicionales del 2.083% mensualmente después
La consolidación está sujeta a empleo continuo. Las concesiones de inducción fueron aprobadas por la Junta Directiva de Acrivon en conformidad con la Regla 5635(c)(4) de Nasdaq y sirven como un incentivo material para el empleo.
Acrivon Therapeutics (Nasdaq: ACRV), 임상 단계의 정밀 의학 회사,는 특정 직원들을 위한 2023 유인 계획하의 주식 보상을 승인했다고 발표했습니다. 이 보상은 2024년 10월 15일에 부여되며, 총 61,950주를 구매할 수 있는 주식 옵션으로 구성됩니다.
주식 옵션은 다음 일정에 따라 귀속됩니다:
- 각 직원의 고용 시작일이 지나고 첫 번째 달의 첫날의 첫 번째 기념일에 25%
- 그 이후 매달 2.083% 추가 분할
귀속은 지속적인 고용에 따라 달라집니다. 유인 부여는 Nasdaq 규칙 5635(c)(4)에 따라 Acrivon의 이사회의 승인을 받았으며, 고용에 대한 중요한 유인책으로 작용합니다.
Acrivon Therapeutics (Nasdaq: ACRV), une entreprise de médecine de précision en phase clinique, a annoncé l'approbation de récompenses en actions dans le cadre de son Plan d'Incitation 2023 pour certains employés. Les récompenses, accordées le 15 octobre 2024, consistent en options d'achat pour un total de 61 950 actions ordinaires d'Acrivon.
Les options d'achat seront acquises selon le calendrier suivant :
- 25 % à la première date anniversaire du premier jour du mois suivant la date d'embauche effective de chaque employé
- Des versements supplémentaires de 2,083 % mensuellement par la suite
L'acquisition est soumise à une poursuite de l'emploi. Les concessions d'incitation ont été approuvées par le conseil d'administration d'Acrivon conformément à la règle 5635(c)(4) de Nasdaq et constituent un véritable incitatif à l'emploi.
Acrivon Therapeutics (Nasdaq: ACRV), ein Unternehmen für Präzisionsmedizin in klinischer Phase, hat die Genehmigung von Aktienvergütungen im Rahmen seines Induktionsplans 2023 für bestimmte Mitarbeiter bekannt gegeben. Die Vergütungen, gewährt am 15. Oktober 2024, bestehen aus Aktienoptionen zum Erwerb von insgesamt 61.950 Aktien des Stammkapitals von Acrivon.
Die Aktienoptionen werden gemäß dem folgenden Zeitplan ausgegeben:
- 25% am ersten Jahrestag des ersten Tages des Monats nach dem jeweiligen Beschäftigungsbeginn jedes Mitarbeiters
- Zusätzliche Raten von 2,083% monatlich danach
Die Vesting erfolgt unter der Voraussetzung einer fortgesetzten Beschäftigung. Die Induktionsgaben wurden vom Vorstand von Acrivon gemäß der Nasdaq-Regel 5635(c)(4) genehmigt und dienen als erhebliches Anreizmittel für die Beschäftigung.
- Granting of stock options may help attract and retain talent
- Compliance with Nasdaq rules for inducement grants
- Potential dilution of existing shareholders' equity
WATERTOWN, Mass., Oct. 16, 2024 (GLOBE NEWSWIRE) -- Acrivon Therapeutics, Inc. (“Acrivon” or “Acrivon Therapeutics”) (Nasdaq: ACRV), a clinical stage precision medicine company utilizing its Acrivon Predictive Precision Proteomics (AP3) platform for the discovery, design, and development of drug candidates through a mechanistic match to patients whose disease is predicted sensitive to the specific treatment, today announced that the company approved a grant of equity awards under its 2023 Inducement Plan to certain employees. The equity awards were granted in the form of stock options and have a grant date of October 15, 2024.
The employees received an aggregate of options to purchase 61,950 shares of Acrivon common stock. The stock options will vest
The inducement grants were approved by Acrivon’s Board of Directors, as required by Nasdaq Rule 5635(c)(4), and were granted as a material inducement to employment in accordance with Nasdaq Rule 5635(c)(4).
About Acrivon Therapeutics
Acrivon is a clinical stage biopharmaceutical company developing precision oncology medicines that it matches to patients whose tumors are predicted to be sensitive to each specific medicine by utilizing Acrivon’s proprietary proteomics-based patient responder identification platform, Acrivon Predictive Precision Proteomics, or AP3. The AP3 platform is engineered to measure compound-specific effects on the entire tumor cell protein signaling network and drug-induced resistance mechanisms in an unbiased manner. These distinctive capabilities enable AP3’s direct application for drug design optimization for monotherapy activity, the identification of rational drug combinations, and the creation of drug-specific proprietary OncoSignature companion diagnostics that are used to identify the patients most likely to benefit from Acrivon’s drug candidates. Acrivon is currently advancing its lead candidate, ACR-368 (also known as prexasertib), a selective small molecule inhibitor targeting CHK1 and CHK2 in a potentially registrational Phase 2 trial across multiple tumor types. The company has received Fast Track designation from the Food and Drug Administration, or FDA, for the investigation of ACR-368 as monotherapy based on OncoSignature-predicted sensitivity in patients with platinum-resistant ovarian or endometrial cancer. Acrivon’s ACR-368 OncoSignature test, which has not yet obtained regulatory approval, has been extensively evaluated in preclinical studies, including in two separate, blinded, prospectively-designed studies on pretreatment tumor biopsies collected from past third-party Phase 2 trials in patients with ovarian cancer treated with ACR-368. The FDA has granted Breakthrough Device designation for the ACR-368 OncoSignature assay for the identification of ovarian cancer patients who may benefit from ACR-368 treatment. The company reported positive clinical data for ovarian and endometrial cancers in April 2024, and in September 2024 it reported additional positive clinical data for endometrial cancer, including a confirmed overall response rate of
In addition to ACR-368, Acrivon is also leveraging its proprietary AP3 precision medicine platform for developing its co-crystallography-driven, internally-discovered pipeline programs. These include ACR-2316, the company’s second clinical stage asset, a potent, selective WEE1/PKMYT1 inhibitor designed for superior single-agent activity as demonstrated in preclinical studies against benchmark inhibitors. The company is also progressing internally- developed preclinical programs, including a cell cycle program with an undisclosed target.
Acrivon has developed AP3 Interactome, a proprietary, computational analytics platform driven by machine learning for integrated comprehensive analyses across all large, in-house AP3 phosphoproteomic drug profiling data sets to advance its in-house research programs.
Forward-Looking Statements
This press release includes certain disclosures that contain “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995 about us and our industry that involve substantial risks and uncertainties. All statements other than statements of historical facts contained in this press release, including statements regarding our future results of operations or financial condition, business strategy and plans and objectives of management for future operations, are forward-looking statements. In some cases, you can identify forward-looking statements because they contain words such as “anticipate,” “believe,” “contemplate,” “continue,” “could,” “estimate,” “expect,” “intend,” “may,” “plan,” “potential,” “predict,” “project,” “should,” “target,” “will,” or “would” or the negative of these words or other similar terms or expressions. Forward-looking statements are based on Acrivon’s current expectations and are subject to inherent uncertainties, risks and assumptions that are difficult to predict. Factors that could cause actual results to differ include, but are not limited to, risks and uncertainties that are described more fully in the section titled “Risk Factors” in our reports filed with the Securities and Exchange Commission. Forward-looking statements contained in this press release are made as of this date, and Acrivon undertakes no duty to update such information except as required under applicable law.
Investor and Media Contacts:
Adam D. Levy, Ph.D., M.B.A.
alevy@acrivon.com
Alexandra Santos
asantos@wheelhouselsa.com
FAQ
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