4DMT Announces New Employment Inducement Grants
4D Molecular Therapeutics (Nasdaq: FDMT), a late-stage biotechnology company, has granted 4,600 Restricted Stock Units (RSUs) to one new non-executive employee on July 8, 2025. The RSUs were awarded under the Company's 2025 Employment Inducement Award Plan, which was established in February 2025 in accordance with Nasdaq Global Market Rule 5635(c)(4) to incentivize new employee recruitment.
4D Molecular Therapeutics (Nasdaq: FDMT), un'azienda biotecnologica in fase avanzata, ha assegnato 4.600 Unità Azionarie Vincolate (RSU) a un nuovo dipendente non esecutivo il 8 luglio 2025. Le RSU sono state concesse nell'ambito del Piano di Incentivi per l'Assunzione 2025 della Società, istituito a febbraio 2025 in conformità con la Regola 5635(c)(4) del Nasdaq Global Market, al fine di favorire il reclutamento di nuovi dipendenti.
4D Molecular Therapeutics (Nasdaq: FDMT), una empresa biotecnológica en etapa avanzada, ha otorgado 4,600 Unidades de Acciones Restringidas (RSU) a un nuevo empleado no ejecutivo el 8 de julio de 2025. Las RSU fueron concedidas bajo el Plan de Incentivos por Contratación 2025 de la Compañía, establecido en febrero de 2025 conforme a la Regla 5635(c)(4) del Nasdaq Global Market para fomentar la contratación de nuevos empleados.
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4D Molecular Therapeutics (Nasdaq : FDMT), une entreprise biotechnologique en phase avancée, a attribué 4 600 unités d’actions restreintes (RSU) à un nouvel employé non cadre le 8 juillet 2025. Les RSU ont été accordées dans le cadre du Plan d’incitation à l’emploi 2025 de la société, établi en février 2025 conformément à la règle 5635(c)(4) du Nasdaq Global Market, afin de stimuler le recrutement de nouveaux employés.
4D Molecular Therapeutics (Nasdaq: FDMT), ein Biotechnologieunternehmen in der Spätphase, hat am 8. Juli 2025 einem neuen nicht geschäftsführenden Mitarbeiter 4.600 Restricted Stock Units (RSUs) gewährt. Die RSUs wurden im Rahmen des 2025 Employment Inducement Award Plans des Unternehmens vergeben, der im Februar 2025 gemäß der Nasdaq Global Market Regel 5635(c)(4) eingerichtet wurde, um die Rekrutierung neuer Mitarbeiter zu fördern.
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EMERYVILLE, Calif., July 11, 2025 (GLOBE NEWSWIRE) -- 4D Molecular Therapeutics (Nasdaq: FDMT, 4DMT or the Company), a leading late-stage biotechnology company advancing durable and disease-targeted therapeutics with potential to transform treatment paradigms and provide unprecedented benefits to patients, today announced that on July 8, 2025, the compensation committee of the Company’s board of directors granted one new non-executive employee 4,600 Restricted Stock Units (RSUs). The RSUs were granted pursuant to the Company’s 2025 Employment Inducement Award Plan, which was approved by the Company’s board of directors in February 2025 under Rule 5635(c)(4) of The Nasdaq Global Market for equity grants to induce new employees to enter into employment with the Company.
About 4DMT
4DMT is a leading late-stage biotechnology company advancing durable and disease-targeted therapeutics with potential to transform treatment paradigms and provide unprecedented benefits to patients. The Company’s lead product candidate 4D-150 is designed to be a backbone therapy forming the foundation of treatment of blinding retinal vascular diseases by providing multi-year sustained delivery of anti-VEGF (aflibercept and anti-VEGF-C) with a single, safe, intravitreal injection, which substantially reduces the treatment burden associated with current bolus injections. The Company’s lead indication for 4D-150 is wet age-related macular degeneration, which is currently in Phase 3 development, and second indication is diabetic macular edema. The Company’s second product candidate is 4D-710, which is the first known genetic medicine to demonstrate successful delivery and expression of the CFTR transgene in the lungs of people with cystic fibrosis after aerosol delivery. 4D Molecular Therapeutics�, 4DMT�, Therapeutic Vector Evolution�, and the 4DMT logo are trademarks of 4DMT.
All of the Company’s product candidates are in clinical or preclinical development and have not yet been approved for marketing by the U.S. Food and Drug Administration or any other regulatory authority. No representation is made as to the safety or effectiveness of the Company’s product candidates for the therapeutic uses for which they are being studied.
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