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Galectin Therapeutics Inc.Informe acción NasdaqCM:GALT

Capitalización bursátil US$136.9m
Precio de las acciones
US$2.21
US$11
79.9% infravalorado descuento intrínseco
1Y72.7%
7D-0.9%
Valor de la cartera
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Galectin Therapeutics Inc.

Informe acción NasdaqCM:GALT

Capitalización de mercado: US$136.9m

Galectin Therapeutics (GALT) Resumen de Acciones

Galectin Therapeutics Inc, empresa biofarmacéutica en fase clínica, se dedica al desarrollo de fármacos para crear nuevas terapias contra las enfermedades fibróticas y el cáncer. Saber más

Análisis fundamental de GALT
Puntuación del snowflake
Valoración0/6
Crecimiento futuro0/6
Rendimiento pasado0/6
Salud financiera0/6
Dividendos0/6

Análisis de riesgos

Patrimonio neto negativo

Tiene menos de 1 año de cash runway

Tiene unos ingresos inferiores a 1 millón de dólares ($0)

Actualmente no es rentable y no se prevé que lo sea en los próximos 3 años

+ 1 riesgos adicionales

GALT Community Fair Values

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Competidores de Galectin Therapeutics Inc.

Historial de precios y rendimiento

Resumen de las cotizaciones máximas, mínimas y variaciones del Galectin Therapeutics
Precios históricos de las acciones
Precio actual de la acciónUS$2.21
Máximo en las últimas 52 semanasUS$7.13
Mínimo de 52 semanasUS$1.22
Beta0.45
Cambio en 1 mes-3.49%
Variación en 3 meses-24.57%
Cambio de 1 año72.66%
Variación en 3 años24.16%
Variación en 5 años-46.10%
Variación desde la OPV-81.58%

Noticias y actualizaciones recientes

Recent updates

Seeking Alpha • Oct 12

Galectin rises as FDA approves to begin human trial of combination immunotherapy in head and neck cancer

Galectin Therapeutics (NASDAQ:GALT) said on Wednesday it had filed an investigational New Drug application with the U.S. Food and Drug Administration for belapectin in combination with a checkpoint inhibitor to treat Head and Neck cancer. (GALT) has risen 3.7% premarket. The company said it also received a study may proceed letter for a Phase 2 clinical trial of Belapectin in combination with Pembrolizumab as first-line treatment in subjects with recurrent/metastatic PD-L1 Positive Squamous Cell Carcinoma of the Head and Neck.
Seeking Alpha • Aug 15

Galectin Therapeutics GAAP EPS of -$0.16

Galectin Therapeutics press release (NASDAQ:GALT): Q2 GAAP EPS of -$0.16. As of June 30, 2022, the Company had $24.2M of cash and cash equivalents. The company believes it has sufficient cash, including availability under its new $60M line of credit, to fund currently planned operations and research and development activities through at least December 31, 2024.
Seeking Alpha • Jul 11

Galectin: Ability To Potentially Target Unmet Medical Need

Results from the phase 3 NAVIGATE study using Belapectin for the treatment of patients with NASH Cirrhosis without esophageal varices are expected in Q1 of 2024. If the primary endpoint of the phase 3 NAVIGATE study is met, ability to advance Belapectin towards other indications such as Pulmonary arterial hypertension, advanced NASH fibrosis, and Lung/Kidney disease. An IND filing to initiate a randomized placebo controlled phase 2 study using Belapectin plus Keytruda for the treatment of patients with Head & Neck cancer is expected in 2022. Galectin had $39.6 million in cash as of December 31, 2021; enough cash to fund its operations until at least March 31, 2023. Galectin Therapeutics Inc. (GALT) is a great speculative biotech play to look into. That's because it is focused on a population with a huge unmet medical need. It is currently enrolling and treating non-alcoholic steatohepatitis ((NASH)) cirrhosis patients with its Belapectin drug in a phase 3 study known as NAVIGATE. A prior phase 2 study established proof of concept in a subpopulation of NASH cirrhosis patients with varices. That is, the drug worked well in this specific patient population. However, when looking at the overall NASH cirrhosis population the entire trial failed. The thing is that if this study ends up succeeding, it would establish proof of concept in using Belapectin as an anti-fibrotic treatment towards other indications such as: Lung/Kidney disease, advanced NASH fibrosis, pulmonary arterial hypertension ((PAH)) and many others. What is also good about Belapectin is that it can also be advanced for oncology as well. As such, Galectin Therapeutics has already selected to advance this drug in combination with Keytruda for the treatment of patients with head and neck cancer. It intends to file an IND in 2022 to initiate a more advanced phase 2 study just focused on using this combination to treat this patient population. Based on the potential with Belapectin as an anti-fibrotic drug, plus the ability to possibly expand into oncology, these are the reasons why I believe that Galectin Therapeutics is a great speculative biotech play to look into. Belapectin For The Treatment Of Patients With NASH Cirrhosis & Other Fibrotic Disorders The main program in the pipeline is the use of Belapectin for the treatment of patients with NASH Cirrhosis. Cirrhosis occurs when the scarring (fibrosis) of the liver is at a late stage in the cycle. The liver is severely injured and it keeps trying to repair itself. It can be caused by many things, like Hepatitis and chronic alcohol drinking. Another item that has been prevalent is eating a lot of fats. What do I mean by this? Well, as I will explain below, Galectin Therapeutics is also going after NASH fibrosis. People who obtain non-alcoholic fatty liver disease ((NAFLD)) can develop Non-alcoholic steatohepatitis ((NASH)). If the inflammation and scarring of the liver becomes far more severe, then that becomes cirrhosis. Cirrhosis is a major problem and may eventually lead to liver failure. Another item to note is that the company ran a proof of concept study known as NASH-CX, which I will talk about below in detail. However, it only saw a benefit of patients of NASH cirrhosis for 50% of the population. More about this below, but just know that this program has massive potential. Galectin was able to show that Belapectin was able to help about 50% of the NASH cirrhosis population it treated. This accomplishment was observed from the phase 2b NASH-CX trial. This is a study that treated up to 162 patients with NASH cirrhosis who were randomized to receive either Belapectin or placebo. The breakdown of the dosing was as follows: 2 mg/kg of belapectin 8 mg/kg of belapectin Placebo Patients receive one of these doses for a total of 62 weeks. The thing to note is that this proof of concept study heavily focused on well-compensated NASH cirrhosis and not decompensated NASH cirrhosis. What's the difference between well-compensated cirrhosis and decompensated NASH cirrhosis? In compensated NASH cirrhosis patients are somewhat functioning albeit not that great. These patients don't have symptoms and their liver does still function. For those with decompensated NASH cirrhosis, the liver is heavily damaged and is not working much if at all. It is said that when a patient is diagnosed with decompensated NASH cirrhosis, they have a life expectancy between 1 and 3 years. That's why the company recruited patients who did have NASH cirrhosis but had not yet reached to decompensated status. The primary endpoint of the study was a reduction in HVPG. HVPG stands for Hepatic venous pressure gradient. It is used to measure the portal hypertension of the liver. That is the vein that carries blood from the digestion organs to the liver. When this is under pressure, it means the disease is far more advanced. The goal of Belapectin is to reduce this measure. The final end result was that 50% patients given Belapectin had achieved a significant reduction in HVPG compared to placebo. That is, those who took 2 mg/kg Belapectin had achieved a 44% reduction, compared to only 15% for those on placebo. This gave a statistically significant p-value of p=0.02. However, the main thing to point out is that this was for patients without varices. What is varices? Basically, varices means an enlarged vein in the liver that is blocked. For the other 50% of patients with varices, Belapectin did not achieve statistical significance. In my opinion, at least the company can still target 50% of the cirrhosis population. Of course, that is that the ongoing late-stage study pans out. The statistical significance of using Belapectin to treat NASH cirrhosis patients was very good. Good enough that the FDA had allowed Galectin to initiate a late-stage phase 2b/3 study known as NAVIGATE. This study intends to enroll up to 315 NASH patients with NASH cirrhosis without esophageal varices. The goal is to attempt to prevent varices from even forming in the liver in the first place. Patients are going to be given either 2 mg/kg of Belapectin , 4 mg/kg of Belapactin or placebo. This phase 2b/3 study was initiated back in June of 2020. As you guessed, the primary endpoint will be to determine the number of varices formed at the end of the treatment period. The less varices developed with patients given belapectin compared to placebo, the greater chance that the study will succeed. As long as belapectin achieves statistical significance for this patient population over placebo, then that opens the door to other fibrotic indications. The company notes that it intends to possibly seek for accelerated approval and may even seek a partnership to help fund it commercially should it need to eventually be marketed. The biggest downside, though, is that this study is a long one. That's because the expected completion date of the study itself is not expected until June of 2023. Thus, interim results from this late-stage NAVIGATE study won't be released until around Q1 of 2024. Financials According to the 10-Q SEC Filing, Galectin Therapeutics had cash and cash equivalents of $39.6 million as of December 31, 2021. However, it received $10 million in proceeds from an unsecured convertible promissory note from its Board Chairman Richard E. Uihlein. I don't think it needs to worry about funding too much, especially with the amount of cash this Board Chairman has put in. It is said that Galectin received a total of $30 million in unsecured promissory notes from Mr. Uihlein in 2021. Not only that, but because its program is highly focused on Belapectin in the ongoing phase 3 NAVIGATE study, it believes it has enough cash to fund its operations until March 31, 2023. Around that point, it will need to obtain additional funding. If it can't get any more cash from Mr. Uihlein again, then I believe it will just have the typical biotech option of selling shares of its common stock on the open market to obtain funding. If it does need to go this route, my guess is that it won't need to do so until the end of 2022. Risks To Business There are several risks that investors should be aware of before taking a position in this speculative biotech. The first risk relates to the phase 3 NAVIGATE trial itself using Belapectin for the treatment of patients with NASH cirrhosis without esophageal varices. Even though the phase 2 study established statistical significance for Belpectin in this subpopulation of NASH cirrhosis patients, there is no guarantee that the same will be achieved in the NAVIGATE trial. If the study fails, not only do I predict that the stock will trade below $1 per share, but also that it will force it to move all its efforts towards oncology.
Seeking Alpha • Jul 01

Galectin: Pursuing A Subset In The NASH Space

Galectin failed a phase 2 trial in 2017. However, the trial saw certain interesting features in a subset of patients. Galectin is pursuing this subset in another trial.
Artículo de análisis • Feb 25

Read This Before Buying Galectin Therapeutics, Inc. (NASDAQ:GALT) Shares

It is not uncommon to see companies perform well in the years after insiders buy shares. On the other hand, we'd be...
Artículo de análisis • Jan 21

Is Galectin Therapeutics (NASDAQ:GALT) In A Good Position To Deliver On Growth Plans?

Even when a business is losing money, it's possible for shareholders to make money if they buy a good business at the...
Artículo de análisis • Dec 09

How Much Of Galectin Therapeutics, Inc. (NASDAQ:GALT) Do Insiders Own?

Every investor in Galectin Therapeutics, Inc. ( NASDAQ:GALT ) should be aware of the most powerful shareholder groups...

Rentabilidad de los accionistas

GALTUS BiotechsMercado US
7D-0.9%-3.0%-0.3%
1Y72.7%32.9%26.7%

Rentabilidad vs. Industria: GALT superó a la industria US Biotechs, que obtuvo un rendimiento del 32.9% el año pasado.

Rentabilidad vs. Mercado: GALT superó al mercado US, que obtuvo un rendimiento del 26.7% el año pasado.

Volatilidad de los precios

Is GALT's price volatile compared to industry and market?
GALT volatility
GALT Average Weekly Movement11.2%
Biotechs Industry Average Movement10.9%
Market Average Movement7.2%
10% most volatile stocks in US Market16.2%
10% least volatile stocks in US Market3.2%

Precio estable de las acciones: El precio de las acciones de GALT ha sido volátil durante los últimos 3 meses en comparación con el mercado US.

Volatilidad a lo largo del tiempo: La volatilidad semanal de GALT(11%) se ha mantenido estable durante el último año, pero sigue siendo superior al 75% de las acciones de US.

Acerca de la empresa

FundadaEmpleadosCEOPágina web
20009Joel Lewisgalectintherapeutics.com

Galectin Therapeutics Inc, empresa biofarmacéutica en fase clínica, se dedica al desarrollo de fármacos para crear nuevas terapias contra las enfermedades fibróticas y el cáncer. El principal producto candidato de la empresa es la belapectina (GR-MD-02), un inhibidor de la galectina 3, que se encuentra en un estudio clínico de fase 2 en pacientes de MASH con fibrosis avanzada y en un segundo ensayo clínico de fase 2b en pacientes de MASH con cirrosis compensada e hipertensión portal. Tiene una empresa conjunta con SBH Sciences, Inc. para investigar y desarrollar pequeños inhibidores de moléculas orgánicas de la galectina-3 para administración oral.

Resumen de fundamentos de Galectin Therapeutics Inc.

¿Cómo se comparan los beneficios e ingresos de Galectin Therapeutics con su capitalización de mercado?
Estadísticas fundamentales de GALT
Capitalización bursátilUS$136.92m
Beneficios(TTM)-US$26.38m
Ingresos (TTM)n/a
0.0x
Ratio precio-ventas (PS)
-5.5x
Ratio precio-beneficio (PE)

¿Está GALT sobrevalorada?

Ver valor justo y análisis de valoración

Beneficios e Ingresos

Estadísticas clave de rentabilidad del último informe de resultados (TTM)
Cuenta de resultados (TTM) de GALT
IngresosUS$0
Coste de los ingresosUS$0
Beneficio brutoUS$0
Otros gastosUS$26.38m
Beneficios-US$26.38m

Últimos beneficios comunicados

Mar 31, 2026

Próxima fecha de beneficios

n/a

Beneficios por acción (BPA)-0.40
Margen bruto0.00%
Margen de beneficio neto0.00%
Ratio deuda/patrimonio-104.2%

¿Cómo se ha desempeñado GALT a largo plazo?

Ver rendimiento histórico y comparativa

Análisis de la empresa y estado de los datos financieros

DatosÚltima actualización (huso horario UTC)
Análisis de la empresa2026/05/20 06:01
Precio de las acciones al final del día2026/05/20 00:00
Beneficios2026/03/31
Ingresos anuales2025/12/31

Fuentes de datos

Los datos utilizados en nuestro análisis de empresas proceden de S&P Global Market Intelligence LLC. Los siguientes datos se utilizan en nuestro modelo de análisis para generar este informe. Los datos están normalizados, lo que puede introducir un retraso desde que la fuente está disponible.

PaqueteDatosMarco temporalEjemplo Fuente EE.UU. *
Finanzas de la empresa10 años
  • Cuenta de resultados
  • Estado de tesorería
  • Balance
Estimaciones del consenso de analistas+3 años
  • Previsiones financieras
  • Objetivos de precios de los analistas
Precios de mercado30 años
  • Precios de las acciones
  • Dividendos, escisiones y acciones
Propiedad10 años
  • Accionistas principales
  • Información privilegiada
Gestión10 años
  • Equipo directivo
  • Consejo de Administración
Principales avances10 años
  • Anuncios de empresas

* Ejemplo para valores de EE.UU., para no EE.UU. se utilizan formularios y fuentes normativas equivalentes.

A menos que se especifique lo contrario, todos los datos financieros se basan en un periodo anual, pero se actualizan trimestralmente. Esto se conoce como datos de los últimos doce meses (TTM) o de los últimos doce meses (LTM). Más información.

Modelo de análisis y copo de nieve

Los detalles del modelo de análisis utilizado para generar este informe están disponibles en nuestra página de Github, también tenemos guías sobre cómo utilizar nuestros informes y tutoriales en Youtube.

Conozca al equipo de talla mundial que diseñó y construyó el modelo de análisis Simply Wall St.

Métricas industriales y sectoriales

Simply Wall St calcula cada 6 horas nuestras métricas sectoriales y de sección. Los detalles de nuestro proceso están disponibles en Github.

Fuentes analistas

Galectin Therapeutics Inc. está cubierta por 5 analistas. 1 de esos analistas presentaron las estimaciones de ingresos o ganancias utilizadas como datos para nuestro informe. Las estimaciones de los analistas se actualizan a lo largo del día.

AnalistaInstitución
Keay NakaeAscendiant Capital Markets LLC
Mayank MamtaniB. Riley Securities, Inc.
Matthew KellerH.C. Wainwright & Co.