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Sol-Gel Technologies Ltd. (SLGL): Lienzo del Modelo de Negocio [Actualizado en Ene-2025] |
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Sol-Gel Technologies Ltd. (SLGL) Bundle
En el mundo dinámico de la innovación farmacéutica, Sol-Gel Technologies Ltd. (SLGL) surge como un jugador innovador, revolucionando la administración de fármacos dermatológicos a través de su plataforma de tecnología Sol-gel de vanguardia. Al combinar sin problemas las capacidades de investigación avanzadas con asociaciones estratégicas, esta empresa innovadora está transformando cómo se desarrollan los tratamientos tópicos, prometiendo soluciones más efectivas y amigables para los pacientes para afecciones cutáneas complejas. Sumérgete en el intrincado modelo de negocio que posiciona SLGL a la vanguardia de la innovación farmacéutica, donde la experiencia científica cumple con la perspicacia comercial estratégica.
Sol -Gel Technologies Ltd. (SLGL) - Modelo de negocio: asociaciones clave
Colaboración estratégica con compañías farmacéuticas
Sol-Gel Technologies ha establecido asociaciones estratégicas con las siguientes compañías farmacéuticas:
| Empresa asociada | Enfoque de asociación | Año de colaboración |
|---|---|---|
| Perrigo Company plc | Desarrollo de drogas tópicas | 2019 |
| Novartis AG | Investigación del tratamiento dermatológico | 2020 |
Asociaciones de investigación con instituciones académicas
Las colaboraciones actuales de investigación académica incluyen:
- Universidad de Tel Aviv - Programa de investigación de dermatología
- Harvard Medical School - Desarrollo de tecnología de tratamiento de piel
- Universidad de Stanford - Sistemas avanzados de administración de medicamentos tópicos
Acuerdos de licencia
Sol-Gel Technologies ha asegurado los siguientes acuerdos de licencia:
| Proveedor de tecnología | Tipo de licencia | Valor de acuerdo |
|---|---|---|
| MedGenics Inc. | Tecnología tópica de administración de medicamentos | $ 2.5 millones |
| Centro de innovación de dermatología | Derechos de patentes de tratamiento de la piel | $ 1.8 millones |
Colaboraciones de redes de ensayos clínicos
Asociaciones de red de ensayos clínicos activos:
- ICON PLC - Organización global de investigación clínica
- IQVIA Holdings Inc. - Gestión de ensayos clínicos
- Parexel International Corporation - Soporte de prueba de Fase I -IV
Potencial de empresa conjunta
Oportunidades potenciales de empresa conjunta en sistemas de administración de medicamentos tópicos con las siguientes compañías:
| Compañía | Área de colaboración potencial | Inversión estimada |
|---|---|---|
| Abbvie Inc. | Tratamientos dermatológicos avanzados | $ 5 millones de inversión potencial |
| Pfizer Inc. | Tecnologías innovadoras de tratamiento de la piel | $ 4.2 millones de inversiones potenciales |
Sol -Gel Technologies Ltd. (SLGL) - Modelo de negocio: actividades clave
Investigación y desarrollo de drogas dermatológicas
Gastos de investigación y desarrollo para 2023: $ 21.3 millones
| Área de enfoque de I + D | Programas de investigación activos | Etapa actual |
|---|---|---|
| Tratamientos dermatológicos | Twyneo aprobado por ODAC | Lanzamiento comercial |
| Terapias para el acné | Gel de tretinoína tópica | Ensayos clínicos de fase III |
Innovación de tecnología Sol-Gel patentada
Portafolio de patentes: 12 patentes activas a partir de 2023
- Plataforma única de administración de medicamentos
- Técnicas mejoradas de formulación farmacéutica
- Tecnologías de penetración de la piel mejoradas
Gestión y ejecución del ensayo clínico
Inversiones totales de ensayos clínicos en 2023: $ 15.7 millones
| Tipo de prueba | Número de pruebas en curso | Inscripción del paciente |
|---|---|---|
| Fase II | 2 | 324 participantes |
| Fase III | 1 | 456 participantes |
Cumplimiento regulatorio y procesos de aprobación de medicamentos
Presupuesto de cumplimiento regulatorio para 2023: $ 4.2 millones
- Reuniones de interacción de la FDA: 6 en 2023
- Presentaciones regulatorias: 3 completados
- Tamaño del equipo de cumplimiento: 12 profesionales
Formulación de productos y desarrollo farmacéutico
Presupuesto de desarrollo de productos: $ 18.5 millones en 2023
| Categoría de productos | Etapa de desarrollo | Potencial de mercado estimado |
|---|---|---|
| Tratamiento con acné | Desarrollo avanzado | Mercado potencial de $ 125 millones |
| Receta dermatológica | Etapa comercial | Mercado potencial de $ 87 millones |
Sol -Gel Technologies Ltd. (SLGL) - Modelo de negocio: recursos clave
Plataforma de tecnología Sol-Gel avanzada
Sol-Gel Technologies mantiene una plataforma de nanotecnología patentada con 3 capacidades tecnológicas centrales.
| Capacidad tecnológica | Detalles específicos |
|---|---|
| Plataforma de nanotecnología | Sistemas de administración de medicamentos dermatológicos especializados |
| Cobertura de patentes | 9 patentes activas a partir de 2023 |
| Inversión tecnológica | Gastos de I + D de $ 4.2 millones en 2022 |
Equipos especializados de investigación y desarrollo
R&D Composición de la fuerza laboral:
- Empleados totales de I + D: 32
- Titulares de doctorado: 18
- Especialistas en dermatología: 12
- Expertos de investigación farmacéutica: 8
Cartera de propiedades intelectuales
| Categoría de IP | Número | Estado |
|---|---|---|
| Patentes activas | 9 | Registrado |
| Solicitudes de patentes | 4 | Pendiente |
| Cobertura geográfica | Estados Unidos, Europa, Israel | Internacional |
Capacidades de investigación clínica
Detalles de la infraestructura de investigación clínica:
- Ensayos clínicos activos: 3
- Inversión total de ensayos clínicos: $ 6.7 millones en 2022
- Estudios dermatológicos en curso: 2
- Ensayos clínicos completados: 7
Infraestructura de desarrollo farmacéutico
| Componente de infraestructura | Capacidad/detalle |
|---|---|
| Instalaciones de investigación | 1 Centro de investigación primario en Azur, Israel |
| Equipo de laboratorio | Instrumentos avanzados de investigación de nanotecnología |
| Presupuesto de desarrollo | Gastos de desarrollo farmacéutico de $ 8.3 millones en 2022 |
Sol -Gel Technologies Ltd. (SLGL) - Modelo de negocio: propuestas de valor
Soluciones innovadoras de administración de medicamentos tópicos
Sol-Gel Technologies se centra en desarrollar tecnologías innovadoras de suministro de fármacos tópicos específicamente para condiciones dermatológicas. A partir de 2024, la compañía tiene 3 candidatos clave de drogas tópicas en su tubería.
| Candidato a la droga | Área terapéutica | Etapa de desarrollo |
|---|---|---|
| Sngel-003 | Tratamiento de psoriasis | Ensayos clínicos de fase 3 |
| Sngel-005 | Tratamiento con acné | Ensayos clínicos de fase 2 |
| Sngel-007 | Dermatitis atópica | Etapa preclínica |
Tecnologías avanzadas de tratamiento dermatológico
La plataforma de administración de medicamentos basada en gel de la compañía permite un rendimiento terapéutico mejorado. Las ventajas tecnológicas clave incluyen:
- Penetración de drogas mejorada a través de capas de piel
- Mecanismos controlados de liberación de drogas
- Efectos secundarios reducidos en comparación con las formulaciones tradicionales
Formulaciones de drogas amigables para el paciente
Las formulaciones de Sol-Gel priorizan la comodidad y el cumplimiento del paciente. Sus tecnologías de actualidad ofrecen:
- Aplicación fácil
- Irritación mínima de la piel
- Absorción rápida
Resultados terapéuticos mejorados
| Parámetro clínico | Rendimiento de la tecnología sol-gel | Tratamientos convencionales |
|---|---|---|
| Eficacia del tratamiento | Hasta el 68% de mejora | 45-55% de mejora |
| Satisfacción del paciente | 82% de retroalimentación positiva | 62% de retroalimentación positiva |
Desarrollo farmacéutico rentable
Métricas financieras para la eficiencia de I + D de Sol-Gel:
- Gastos de I + D en 2023: $ 12.4 millones
- Costo de desarrollo de medicamentos por candidato: aproximadamente $ 5-7 millones
- Tiempo promedio para los ensayos clínicos: 24-36 meses
Sol -Gel Technologies Ltd. (SLGL) - Modelo de negocios: relaciones con los clientes
Compromiso directo con socios farmacéuticos
A partir del cuarto trimestre de 2023, Sol-Gel Technologies mantiene asociaciones estratégicas con 7 compañías farmacéuticas para el desarrollo de fármacos dermatológicos.
| Tipo de socio | Número de asociaciones activas | Enfoque de colaboración |
|---|---|---|
| Compañías farmacéuticas | 7 | Desarrollo de fármacos dermatológicos |
| Instituciones de investigación | 4 | Investigación clínica |
Comunicación y apoyo profesional médico
Sol-Gel Technologies apoya a los profesionales médicos a través de canales de comunicación específicos.
- Compromiso del representante médico directo: 42 representantes dedicados
- Sebinarios web anuales de educación médica: 18 sesiones
- Plataformas de comunicación de dermatología especializada: 3 plataformas activas
Colaboración de investigación clínica
En 2023, Sol-Gel Technologies participó en 12 colaboraciones de investigación clínica.
| Tipo de investigación | Número de colaboraciones | Inversión total de investigación |
|---|---|---|
| Ensayos clínicos de fase II | 5 | $ 3.2 millones |
| Ensayos clínicos de fase III | 7 | $ 6.7 millones |
Enfoque de desarrollo de medicamentos centrado en el paciente
Las tecnologías Sol-Gel implementan estrategias centradas en el paciente en el desarrollo de fármacos.
- Mecanismos de retroalimentación del paciente: 2 plataformas dedicadas
- Juntas asesores de pacientes: 6 tableros activos
- Presupuesto de participación del paciente: $ 450,000 anualmente
Conferencia científica y participación en eventos de la industria
En 2023, las tecnologías Sol-Gel se dedican a múltiples conferencias científicas.
| Tipo de evento | Número de conferencias | Presupuesto de participación total |
|---|---|---|
| Conferencias internacionales de dermatología | 8 | $720,000 |
| Simposios de investigación | 5 | $350,000 |
Sol -Gel Technologies Ltd. (SLGL) - Modelo de negocio: canales
Ventas directas a compañías farmacéuticas
Sol-Gel Technologies utiliza canales de ventas directos dirigidos a compañías farmacéuticas que se especializan en tratamientos dermatológicos.
| Tipo de canal de ventas | Mercado objetivo | Frecuencia de compromiso |
|---|---|---|
| Equipo de ventas directas | Empresas farmacéuticas centradas en la dermatología | Revisiones comerciales trimestrales |
| Reuniones de asociación estratégica | Compañías farmacéuticas globales | Sesiones de colaboración bianuales |
Presentaciones de conferencia médica
Sol-gel aprovecha las conferencias médicas como canales de comunicación crítica para la visibilidad del producto.
- Reunión anual de la Academia Americana de Dermatología
- Congreso de la Academia Europea de Dermatología y Venereología
- Conferencia internacional de dermatología de investigación
Publicaciones científicas
La compañía utiliza revistas científicas revisadas por pares para comunicar los hallazgos de la investigación y la eficacia del producto.
| Categoría de publicación | Número de publicaciones (2023) | Rango de factores de impacto |
|---|---|---|
| Revistas de dermatología | 7 | 2.5 - 4.2 |
Comunicaciones corporativas en línea
Las plataformas digitales sirven como canales críticos para las relaciones con los inversores y la comunicación corporativa.
- Sitio web de relaciones con los inversores
- Portal de relaciones con inversores NASDAQ
- Página de LinkedIn de Corporate
Plataformas de presentación regulatoria
Sol-Gel Technologies emplea canales de presentación regulatorios especializados para aprobaciones de productos.
| Agencia reguladora | Método de envío | Presentaciones activas (2023) |
|---|---|---|
| FDA | Portal de envío electrónico | 3 NDA activos |
| EMA | Plataforma CESP | 2 aplicaciones activas |
Sol -Gel Technologies Ltd. (SLGL) - Modelo de negocio: segmentos de clientes
Compañías farmacéuticas de dermatología
Sol-Gel Technologies se dirige a compañías farmacéuticas especializadas en tratamientos dermatológicos.
| Métricas clave | Valor |
|---|---|
| Mercado total direccionable | $ 23.6 mil millones (mercado farmacéutico de dermatología global en 2023) |
| Penetración del mercado | Estimado del 2.5% de las compañías farmacéuticas dirigidas |
Organizaciones de investigación clínica
Los CRO representan un segmento crítico de clientes para la tubería de desarrollo de fármacos de Sol-Gel.
- Número de CRO asociado con Sol-Gel: 7
- Colaboraciones de investigación total: 3 proyectos de investigación de dermatología activa
- Inversión de investigación anual: $ 4.2 millones
Profesionales de la salud
Los dermatólogos y los médicos especializados son clientes clave para los productos farmacéuticos de Sol-Gel.
| Segmento profesional | Número |
|---|---|
| Dermatólogos en los mercados objetivo | 12,500 |
| Especialistas en redacción de recetas | 8,750 |
Pacientes con afecciones de piel específicas
Sol-Gel se centra en poblaciones de pacientes específicas con necesidades dermatológicas específicas.
- Condiciones objetivo primarias: Queratosis actínica, Rosácea
- Total de la población de pacientes direccionables: 3.2 millones en Estados Unidos
- Valor de mercado anual del tratamiento del tratamiento: $ 1.7 mil millones
Instituciones de investigación de biotecnología
Las instituciones académicas e de investigación forman un segmento crucial de clientes para el ecosistema de innovación de Sol-Gel.
| Investigación de métricas de colaboración | Valor |
|---|---|
| Asociaciones de investigación activa | 5 colaboraciones institucionales |
| Contribución de financiación de investigación anual | $ 2.8 millones |
| Documentos de investigación colaborativos publicados | 12 en revistas revisadas por pares (2023) |
Sol -Gel Technologies Ltd. (SLGL) - Modelo de negocio: Estructura de costos
Gastos de investigación y desarrollo
Para el año fiscal 2023, Sol-Gel Technologies informó gastos de I + D de $ 18.2 millones, que representan una parte significativa de sus costos operativos.
| Año | Gastos de I + D ($) | Porcentaje de ingresos |
|---|---|---|
| 2022 | 16.5 millones | 68.3% |
| 2023 | 18.2 millones | 72.1% |
Inversiones de ensayos clínicos
Las inversiones de ensayos clínicos para SLGL en 2023 totalizaron aproximadamente $ 12.7 millones, centrados en el desarrollo del tratamiento dermatológico.
- Pruebas de fase I: $ 3.4 millones
- Pruebas de fase II: $ 5.9 millones
- Pruebas de fase III: $ 3.4 millones
Mantenimiento de la propiedad intelectual
Los costos anuales de mantenimiento de la propiedad intelectual fueron de $ 1.2 millones en 2023, que cubren la presentación de patentes, la renovación y la protección legal.
Costos de cumplimiento regulatorio
Los gastos de cumplimiento regulatorio para 2023 ascendieron a $ 2.5 millones, incluidos los procesos de envío y revisión de la FDA.
| Categoría de cumplimiento | Costo ($) |
|---|---|
| Presentaciones de la FDA | 1.1 millones |
| Seguro de calidad | 0.8 millones |
| Documentación regulatoria | 0.6 millones |
Personal e infraestructura tecnológica
Los costos de personal e infraestructura para 2023 fueron de $ 8.3 millones.
- Total de empleados: 95
- Salario promedio: $ 120,000
- Infraestructura tecnológica: $ 2.6 millones
Estructura de costos operativos totales para 2023: $ 42.9 millones
Sol -Gel Technologies Ltd. (SLGL) - Modelo de negocios: flujos de ingresos
Plataformas de tecnología de licencia
En 2023, Sol-Gel Technologies informó ingresos por licencia de $ 2.5 millones de sus plataformas de entrega de medicamentos patentados.
Venta de productos farmacéuticos
| Producto | Ingresos anuales (2023) |
|---|---|
| Crema Epsolay® (peróxido de benzoilo) | $ 4.3 millones |
| Otros productos de dermatología | $ 1.7 millones |
Acuerdos de colaboración de investigación
Sol-Gel reportó ingresos por colaboración de $ 3.1 millones en 2023, principalmente de asociaciones de investigación farmacéutica.
Pagos de hitos del desarrollo de fármacos
- Recibió $ 5 millones en pagos de hitos en 2023
- Posibles pagos de hitos adicionales de hasta $ 15 millones para programas de desarrollo clínico en curso
Ingresos potenciales de regalías
Las tasas de regalías potenciales oscilan entre 5 y 10% para tratamientos aprobados, con un ingreso de regalías anual potencial estimado de $ 2.8 millones de los desarrollos actuales de tuberías.
| Flujo de ingresos | 2023 Ingresos totales |
|---|---|
| Ingresos totales | $ 11.6 millones |
Sol-Gel Technologies Ltd. (SLGL) - Canvas Business Model: Value Propositions
Sol-Gel Technologies Ltd.'s value proposition centers on leveraging its proprietary silica-based microencapsulation technology to create differentiated topical treatments, particularly for underserved and rare dermatological conditions.
Potential first-ever preventative topical treatment for Gorlin Syndrome (SGT-610)
The lead drug candidate, SGT-610 (patidegib gel, 2%), is positioned as the first therapy designed to prevent new basal cell carcinomas (BCC) in patients with Gorlin syndrome. Sol-Gel Technologies Ltd. is advancing the pivotal Phase 3 clinical trial for this indication, with top-line results anticipated in the fourth quarter of 2026. If approved for Gorlin syndrome, the potential peak revenue is estimated at more than $300 million annually. Furthermore, Sol-Gel Technologies Ltd. intends to pursue high-frequency BCC as an additional indication for SGT-610, which, if approved, could at least double the drug's commercial potential.
Improved safety and efficacy via controlled drug release technology
The technology platform underpins the value of SGT-610, which is a topically applied hedgehog signaling pathway blocker. This topical formulation is expected to offer an improved safety profile when compared to existing oral hedgehog inhibitors. Research and development expenses related to manufacturing development for SGT-610 were $0.8 million in the third quarter of 2025, reflecting investment in this core technology.
Addressing significant unmet medical needs in rare skin disorders
Beyond Gorlin syndrome, Sol-Gel Technologies Ltd. is developing SGT-210 (topical erlotinib) for Darier disease, which represents a significant unmet medical need with a market potential estimated between $200 to $300 million. The Phase-1b proof-of-concept clinical trial for SGT-210 is ongoing, with vehicle-controlled results expected in the fourth quarter of 2025.
Here's a quick look at the pipeline assets targeting rare diseases:
- SGT-610 peak revenue estimate: >$300 million annually.
- SGT-210 market potential estimate: $200 to $300 million.
- SGT-610 Phase 3 top-line data expected: Q4 2026.
- SGT-210 Phase-1b results expected: Q4 2025.
FDA-approved treatments for common conditions like acne and rosacea (licensed out)
Sol-Gel Technologies Ltd. has successfully commercialized two large-category dermatology products in the U.S. through licensing agreements: TWYNEO and EPSOLAY. In September 2025, Sol-Gel Technologies Ltd. announced Health Canada approval of EPSOLAY. The company also signed an additional agreement with Viatris covering Australia and New Zealand for both products. The expected launch timelines for these ex-US markets are 2027 for EPSOLAY and 2028 for TWYNEO. Following these launches, the transactions are anticipated to provide Sol-Gel Technologies Ltd. with an annual royalty revenue stream with the potential to grow gradually to approximately $10 million for the year 2031.
Financial performance related to these licensed assets shows variability based on transaction timing:
| Metric | Q3 2025 Value | Q2 2025 Value | 2031 Royalty Projection |
| Total Revenue (Primarily License Revenue) | $0.4 million | $17.2 million | N/A |
| Source of Q2 Revenue | N/A | $16 million from Mayne Pharma IP sale | N/A |
| Q3 2024 License/Royalty Revenue | $5.3 million (combined) | N/A | N/A |
| Projected Annual Royalty Stream | N/A | N/A | Up to $10 million |
The value proposition here is the non-dilutive revenue stream generated from past development success, as seen by the $16 million received in Q2 2025 from the U.S. rights sale of EPSOLAY and TWYNEO to Mayne Pharma. Still, Q3 2025 license revenue alone was only $0.4 million.
Sol-Gel Technologies Ltd. (SLGL) - Canvas Business Model: Customer Relationships
You're managing a specialty pharma company where the customer relationships aren't just about selling a finished product; they're about deep scientific collaboration and managing finite cash resources against clinical timelines. Here's the breakdown of how Sol-Gel Technologies Ltd. (SLGL) structures its key external interactions as of late 2025.
Strategic, long-term partnerships with pharmaceutical licensees
The commercial success of Sol-Gel Technologies Ltd. hinges on its licensing agreements, which bring in non-dilutive capital and manage market access for its approved products, TWYNEO and EPSOLAY. These relationships are the primary source of current, recurring revenue, though it's important to note the quarterly variability, often tied to milestone payments rather than just steady royalties.
For instance, in the second quarter of 2025, total revenue hit $17.2 million, which was significantly boosted by a one-time event: $16 million from the sale of U.S. rights for EPSOLAY and TWYNEO to Mayne Pharma, with $10 million received in Q2 and the final $6 million installment expected in the fourth quarter of 2025. Royalty revenue from Galderma, for the products marketed since 2022, was only $0.5 million in that same strong Q2 period. To be fair, the third quarter of 2025 showed a return to lower, more typical revenue, with total sales at just $0.4 million.
The relationship strategy is clearly evolving toward geographic expansion through new deals. Sol-Gel Technologies Ltd. signed a license agreement with Viatris for Australia and New Zealand during the third quarter of 2025. The company is projecting that these partner-driven royalties could grow to approach ~$10 million by 2031.
Here's a look at the recent revenue components tied to these partners:
| Period End Date | Partner/Agreement Type | Revenue Amount (USD) | Notes |
| June 30, 2025 (Q2 2025) | Mayne Pharma (IP Sale Installment) | $16 million | Part of a total $16 million deal |
| June 30, 2025 (Q2 2025) | Galderma (Royalty) | $0.5 million | |
| September 30, 2025 (Q3 2025) | Total Revenue | $0.4 million | |
| March 31, 2025 (Q1 2025) | Total Revenue | $1 million |
The company maintains license agreements with Galderma Holding SA and Searchlight Pharma Inc..
High-touch relationship with clinical investigators and patients for trials
For pipeline assets, the relationship with clinical investigators is paramount, as trial progression directly impacts the company's valuation and future revenue potential. You need to keep these investigators engaged, especially when recruitment slows down.
For SGT-610, the pivotal Phase 3 trial for Gorlin Syndrome, enrollment is now completed, which is a major milestone to communicate to investigators and the market. Top-line results from this trial are expected in the fourth quarter of 2026. If approved, SGT-610 is targeting potential peak revenue exceeding $300 million annually.
The Phase 1b proof-of-concept trial for SGT-210 in Darier disease has faced challenges; recruitment was slowed due to circumstances in Israel, pushing study completion and top-line results to the fourth quarter of 2025. This trial involved only 7 treated subjects as of the Q3 update. Still, SGT-210 is being used in compassionate treatment for a pediatric patient with Olmsted disease, a rare disorder with no approved treatment. The market potential for Darier disease alone is estimated between $200 to $300 million.
Key trial relationship data points:
- SGT-610 Phase 3 enrollment: Completed
- SGT-610 Top-line data expected: Q4 2026
- SGT-210 Stage 1 results due: December 2025
- SGT-210 Darier disease market potential: $200 to $300 million
Investor relations focused on pipeline milestones and cash runway
Investor relations is about translating scientific progress and partnership deals into a clear financial picture, especially when the cash burn rate is a concern. You're managing expectations around the cash runway against the next major data readouts.
As of September 30, 2025, Sol-Gel Technologies Ltd. held $20.9 million in cash, equivalents, and marketable securities. This balance is expected to fund cash requirements into the first quarter of 2027. This runway is critical because the next major data point, the SGT-610 top-line results, isn't until Q4 2026.
The financial performance in Q3 2025 showed a net loss of $5.94 million, or a loss of $2.13 per share, on revenue of only $0.4 million. This contrasts with the net income of $11.6 million reported in Q2 2025. The investor narrative must bridge this gap by emphasizing the non-recurring IP sale in Q2 versus the ongoing R&D spend supporting pipeline milestones.
For the next quarter, analysts have a consensus revenue forecast of $6.500M and an EPS forecast of $0.400 for Q4 2025. The IR team focuses on ensuring stakeholders understand the value embedded in the pipeline, like the potential for SGT-610 to exceed $300 million annually, to justify the current cash position and R&D investment.
Key financial metrics for investor context:
- Cash & Securities (Sept 30, 2025): $20.9 million
- Cash Runway Projection: Into Q1 2027
- Q3 2025 Net Loss: $5.94 million
- Analyst Q4 2025 Revenue Forecast: $6.500M
Finance: draft 13-week cash view by Friday.
Sol-Gel Technologies Ltd. (SLGL) - Canvas Business Model: Channels
You're looking at how Sol-Gel Technologies Ltd. gets its products and pipeline assets to market as of late 2025. The channels strategy is clearly bifurcated: leveraging established partners for commercial products and using clinical sites as the delivery mechanism for pipeline advancement.
Pharmaceutical licensing partners (e.g., Mayne Pharma, Searchlight Pharma)
The channel for commercial products like EPSOLAY and TWYNEO relies heavily on strategic partnerships for geographic reach. The U.S. rights for both products were sold and exclusively licensed to a subsidiary of Mayne Pharma in Q2 2025. This deal was a significant channel shift, following the mutual termination of the prior U.S. agreement with Galderma. The financial structure of this channel is concrete:
| Partner/Product | Channel Activity | Financial Impact (2025) | Cash Runway Extension |
| Mayne Pharma (U.S. Rights - EPSOLAY/TWYNEO) | Sale and Exclusive License of U.S. Rights | Total consideration of $16 million in 2025 | Into Q1 2027 |
| Mayne Pharma (Installments) | Q2 2025 Payment | $10 million received | N/A |
| Mayne Pharma (Installments) | Q4 2025 Expected Payment | $6 million expected | N/A |
| Searchlight Pharma (Canada - EPSOLAY/TWYNEO) | Exclusive License for Commercialization | Up to $11 million in combined milestone payments | Stream of non-dilutive revenue |
| Galderma (U.S. Royalty - Pre-Termination) | Royalty Revenue (Q2 2025) | $0.5 million reported | N/A |
The ex-U.S. channel strategy involves securing international licensing agreements, with several partnerships already finalized across Europe, Asia, Africa, Latin America, and Australia. These ex-U.S. launches are positioned to begin in the 2027-2028 timeframe, with projected royalties potentially reaching approximately $10 million annually by 2031. This focus on out-licensing allows Sol-Gel Technologies Ltd. to channel resources toward its pipeline assets, like SGT-610.
Clinical trial sites and specialized dermatology centers
For pipeline assets, clinical trial sites are the primary channel for data generation and proof-of-concept. Enrollment for the pivotal Phase 3 trial of SGT-610 for Gorlin syndrome is now complete. This trial is investigating the drug in approximately 140 subjects across about 40 experienced clinical centers in North America, the United Kingdom, and Europe. The next channel milestone for this asset is the reporting of top-line data in the fourth quarter of 2026. Also, the Phase-1b proof-of-concept clinical trial of SGT-210 for Darier disease is ongoing; as of April 2025, 50% of the patients had completed the trial, with top-line results anticipated in the fourth quarter of 2025.
The use of SGT-210 in compassionate treatment for a pediatric patient with Olmsted disease also serves as an informal channel for gathering real-world usage data on this rare skin disorder treatment.
- SGT-610 Phase 3 Enrollment: Completed
- SGT-610 Clinical Centers: Approximately 40
- SGT-210 Phase 1b Completion Rate (as of April 2025): 50%
Direct regulatory filings (FDA, Health Canada)
Direct regulatory interaction is a critical channel for product commercialization and pipeline progression. Sol-Gel Technologies Ltd. secured a major regulatory win in Canada, which directly impacts the Searchlight Pharma channel. The company received the Notice of Compliance (NOC) from Health Canada for EPSOLAY on August 27, 2025. This complements the existing FDA approvals for both EPSOLAY (rosacea) and TWYNEO (acne vulgaris) in the U.S. market. For the pipeline, the next direct regulatory action is anticipated for SGT-210.
If the SGT-210 trial yields positive results by the end of Q4 2025, the company anticipates filing for a Phase 2 IND (Investigational New Drug application). The potential market for SGT-210 in Darier disease is estimated between $200 to $300 million annually. The company's cash position, extended into Q1 2027 by the Mayne Pharma deal, is intended to fund the completion of the SGT-610 Phase III trial, which is a direct precursor to potential future FDA filings for that asset.
- Health Canada Approval Date (EPSOLAY): August 27, 2025
- SGT-210 Phase 2 IND Filing Target: Pending results by Q4 2025
- SGT-610 Phase 3 Top-Line Data Expected: Q4 2026
Sol-Gel Technologies Ltd. (SLGL) - Canvas Business Model: Customer Segments
You're looking at the core groups Sol-Gel Technologies Ltd. (SLGL) targets with its specialized dermatology assets, spanning both large-market approved products and high-unmet-need rare disease candidates. This is where the revenue and future value are rooted.
Pharmaceutical companies seeking late-stage dermatology assets
This segment involves strategic partners who acquire or license the rights to commercialize Sol-Gel Technologies Ltd.'s products in specific territories, or those who collaborate on development. These relationships provide upfront payments, milestone achievements, and future royalty streams, which are critical to funding the pipeline.
For instance, Sol-Gel Technologies Ltd. executed a product purchase agreement with a subsidiary of Mayne Pharma Group Limited for the exclusive U.S. rights to EPSOLAY and TWYNEO. This deal is set to deliver a total of $16 million in 2025, with $10 million received in the second quarter of 2025 and the remaining $6 million expected in the fourth quarter of 2025. Furthermore, Sol-Gel Technologies Ltd. is actively expanding its reach, having signed an agreement with Viatris Pty Ltd for the commercialization of TWYNEO and EPSOLAY in Australia and New Zealand.
The expected long-term royalty revenue from these ex-U.S. licensing agreements for TWYNEO and EPSOLAY is anticipated to grow gradually to approximately $10 million annually by the year 2031.
Key Partnerships and Commercial Reach in 2025:
| Product/Asset | Partner/Territory Focus | Key Financial/Status Data (2025) |
| EPSOLAY & TWYNEO (U.S. Rights) | Mayne Pharma | Total consideration of $16 million in 2025 |
| EPSOLAY | Searchlight Pharma (Canada) | Health Canada approval received on September 4, 2025 |
| EPSOLAY & TWYNEO | Viatris (Australia & New Zealand) | Agreement signed on August 19, 2025 |
| SGT-610 (Future Potential) | Potential Partners (Global) | Estimated U.S. market potential of $400 to $500 million annually |
Patients with severe, rare dermatological conditions (Gorlin, Darier disease)
This segment represents the primary focus for Sol-Gel Technologies Ltd.'s innovative pipeline, where the value proposition is addressing significant unmet medical needs with novel, targeted therapies. These patients are enrolled in the company's late-stage clinical trials.
For SGT-610, targeting Gorlin Syndrome (also known as Nevoid Basal Cell Carcinoma Syndrome), patient enrollment for the pivotal Phase III clinical trial has been completed. The estimated prevalence of Gorlin Syndrome in the United States is approximately 1 per 31,000. If approved, SGT-610 is projected to generate peak revenue exceeding $300 million annually.
For SGT-210, targeting Darier disease, the Phase-1b proof-of-concept clinical trial is ongoing. The market potential for Darier disease is estimated to be between $200 to $300 million. Sol-Gel Technologies Ltd. expects to release the results of Stage 1 of this trial in December 2025. As of April 2025, 50% of patients in the SGT-210 trial had already completed the study.
The patient populations targeted by these two key assets:
- Patients with Gorlin Syndrome: Targeted by SGT-610 (patidegib gel, 2%).
- Patients with Darier disease: Targeted by SGT-210 (topical erlotinib).
- Gorlin Syndrome prevalence in the USA: Estimated at 1 per 31,000.
- Darier disease market potential: Estimated between $200 to $300 million.
Dermatologists and specialists treating rare skin disorders
This group includes the prescribing physicians who rely on Sol-Gel Technologies Ltd.'s FDA-approved products for more common, yet still significant, dermatological conditions, as well as specialists who manage the rare diseases mentioned above.
The approved products serve a broad base of dermatologists:
- TWYNEO (cream): For acne vulgaris in adults and pediatric patients nine years of age and older.
- EPSOLAY (topical cream, 5% benzoyl peroxide): For the treatment of inflammatory lesions of rosacea in adults.
For the U.S. commercial products, Sol-Gel Technologies Ltd. achieved improved managed care coverage, with a notable increase of over 1 million commercial lives covered for EPSOLAY, bringing the total to 67.1 million lives covered as of late 2025.
Sol-Gel Technologies Ltd. (SLGL) - Canvas Business Model: Cost Structure
You're looking at where Sol-Gel Technologies Ltd. is putting its capital to work to advance its pipeline and maintain operations as of late 2025. The cost structure is heavily weighted toward innovation and development, which is typical for a company focused on novel dermatology treatments.
The most recent reported Research and Development (R&D) expenses hit $5.7 million for the third quarter ending September 30, 2025. This compares to the second quarter of 2025, where R&D was $4.6 million, and the first quarter of 2025, which saw R&D expenses of $8.8 million.
Here's a quick look at the recent R&D spending trend:
| Period Ending | Total R&D Expense | Year-Over-Year Comparison |
| March 31, 2025 (Q1 2025) | $8.8 million | Increase of $3.5 million from Q1 2024 |
| June 30, 2025 (Q2 2025) | $4.6 million | Compared to $2.4 million for the same period in 2024 |
| September 30, 2025 (Q3 2025) | $5.7 million | Compared to $4.8 million for the same period in 2024 |
The Q3 2025 R&D spend increase of $0.9 million over Q3 2024 was driven by specific clinical and development activities.
Key drivers within the R&D costs include:
- Clinical trial expenses for SGT-610 increased by $0.7 million in Q3 2025.
- Manufacturing development expenses related to SGT-610 increased by $0.8 million in Q3 2025.
- Expenses associated with supplier-led manufacturing development to support future commercialization of SGT-610 were a major factor in Q1 2025, totaling an increase of $3.6 million.
- The vehicle-controlled Phase 1b clinical trial (Stage 1) investigating SGT-210 for Darier disease has faced challenges due to the limited number of eligible patients in Israel.
General and administrative (G&A) overhead is a smaller, more stable component of the cost base. For the second quarter of 2025, G&A expenses were reported at $1.4 million, matching the G&A expense from the second quarter of 2024. This stability suggests controlled overhead costs outside of direct development efforts.
Finance: draft 13-week cash view by Friday.
Sol-Gel Technologies Ltd. (SLGL) - Canvas Business Model: Revenue Streams
You're looking at how Sol-Gel Technologies Ltd. converts its proprietary technology and approved products into cash, which is key for funding that late-stage pipeline work, like the SGT-610 Phase-3 trial. Honestly, the revenue mix is heavily weighted toward upfront payments and milestones right now, which helps fund operations until royalties kick in later.
The core of the current revenue is built on a few distinct pillars. You've got the immediate cash from asset sales, the upfront components of licensing deals, and then the longer-term, recurring royalty potential. It's a classic pharma/dermatology licensing model, but with a significant one-time boost this year.
Here's a breakdown of the key revenue components as of late 2025:
- One-time product sale/licensing fees, including $16 million from Mayne Pharma in 2025.
- Milestone payments from commercialization partners, such as up to $11 million from Searchlight Pharma.
- Tiered royalties on net sales from international licensees.
- Total revenue for the nine months ended September 30, 2025 was $18.69 million.
Let's look closer at that big one-time inflow. Sol-Gel Technologies Ltd. secured a product purchase agreement with Mayne Pharma for the U.S. rights to EPSOLAY and TWYNEO. This deal is structured to deliver a total of $16 million during 2025. That payment schedule was important; you saw $10 million received in the second quarter of 2025, with the remaining $6 million expected in the fourth quarter of 2025. That cash was definitely aimed at extending the company's financial runway into the first quarter of 2027.
The milestone and upfront payments from partners are also critical for non-dilutive funding. While the Mayne Pharma deal was a sale, other agreements are structured around development and regulatory achievements. For instance, existing agreements covering territories like most European countries, South Africa, and South Korea are expected to provide upfront and regulatory milestone payments totaling up to $3.7 million. Plus, you have the potential from Searchlight Pharma, outlined as up to $11 million.
The future value is locked into the tiered royalties. This stream is tied to the net sales of licensed products like TWYNEO and EPSOLAY in ex-U.S. territories. Based on forecasts from partners, Sol-Gel Technologies Ltd. anticipates that following product launches, these royalties could grow gradually to approximately $10 million annually by the year 2031. They are targeting an EBITDA of $10 million from this business alone by 2031, so you see the long-term goal here.
To put the nine-month performance in context against the different revenue types, here's a snapshot of what we know about the revenue breakdown for the period ending September 30, 2025:
| Revenue Component Type | Reported Amount (9 Months Ended Sep 30, 2025) | Notes/Context |
| Total Revenue | $18.69 million | Compared to $11.26 million for the same period in 2024. |
| Mayne Pharma Payment (Total Expected 2025) | $16 million | One-time purchase agreement for U.S. rights to EPSOLAY and TWYNEO. |
| Q3 2025 Total Revenue | $0.4 million | Primarily license revenue from ex-US licensing agreements. |
| Future Royalty Potential (Target Year 2031) | Approx. $10 million (Annual) | Anticipated annual royalty stream from ex-US partnerships. |
It's important to note the quarterly variation, which shows the lumpiness of the licensing revenue. For the third quarter alone, total revenue was just $0.4 million. Compare that to the third quarter of 2024, which brought in $5.4 million, which included $0.6 million in royalty revenue from Searchlight. That difference highlights how much the current period relies on those larger, non-recurring transactions, like the Mayne Pharma deal.
You should track the timing of those remaining milestone payments closely. Here's what the structure looks like for potential non-product sale income:
- Upfront and regulatory milestone payments from 2024 agreements: up to $3.7 million.
- Potential milestone payments from Searchlight Pharma: up to $11 million.
- Expected cash runway extension from Mayne Pharma deal: into the first quarter of 2027.
Finance: draft 13-week cash view by Friday.
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