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Galectin Therapeutics Inc.NasdaqCM:GALT Rapporto sulle azioni

Cap. di mercato US$136.9m
Prezzo delle azioni
US$2.21
US$11
79.9% sottovalutato sconto intrinseco
1Y72.7%
7D-0.9%
Valore del portafoglio
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Galectin Therapeutics Inc.

Report azionario NasdaqCM:GALT

Capitalizzazione di mercato: US$136.9m

Galectin Therapeutics (GALT) Panoramica del titolo

Galectin Therapeutics Inc. è una società biofarmaceutica in fase clinica, impegnata nello sviluppo di farmaci per creare nuove terapie per le malattie fibrotiche e il cancro. Maggiori dettagli

GALT analisi fondamentale
Punteggio fiocco di neve
Valutazione0/6
Crescita futura0/6
Prestazioni passate0/6
Salute finanziaria0/6
Dividendi0/6

Analisi del rischio

Patrimonio netto negativo

Ha meno di 1 anno di pista di cassa

Realizza un fatturato inferiore a 1 milione di dollari ( $0 )

Attualmente non redditizio e non si prevede che diventerà redditizio nei prossimi 3 anni

+ 1 più rischio

GALT Community Fair Values

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Concorrenti di Galectin Therapeutics Inc.

Storia dei prezzi e prestazioni

Riepilogo dei massimi, dei minimi e delle variazioni dei prezzi delle azioni per Galectin Therapeutics
Prezzi storici delle azioni
Prezzo attuale dell'azioneUS$2.21
Massimo di 52 settimaneUS$7.13
Minimo di 52 settimaneUS$1.22
Beta0.45
Variazione di 1 mese-3.49%
Variazione a 3 mesi-24.57%
Variazione di 1 anno72.66%
Variazione a 3 anni24.16%
Variazione a 5 anni-46.10%
Variazione dall'IPO-81.58%

Notizie e aggiornamenti recenti

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.
Articolo di analisi • 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...
Articolo di analisi • 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...
Articolo di analisi • 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...

Rendimenti per gli azionisti

GALTUS BiotechsUS Mercato
7D-0.9%-4.9%-1.0%
1Y72.7%28.1%23.3%

Ritorno vs Industria: GALT ha superato il US Biotechs che ha restituito 28.1 % nell'ultimo anno.

Rendimento vs Mercato: GALT ha superato il mercato US che ha restituito 23.3 % nell'ultimo anno.

Volatilità dei prezzi

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%

Prezzo delle azioni stabile: Negli ultimi 3 mesi il prezzo delle azioni di GALT è stato volatile rispetto al mercato US.

Volatilità nel tempo: La volatilità settimanale ( 11% ) di GALT è rimasta stabile nell'ultimo anno, ma è comunque superiore al 75% delle azioni US.

Informazioni sull'azienda

FondatoI dipendentiAMMINISTRATORE DELEGATOSito web
20009Joel Lewisgalectintherapeutics.com

Galectin Therapeutics Inc. è una società biofarmaceutica in fase clinica, impegnata nello sviluppo di farmaci per creare nuove terapie per le malattie fibrotiche e il cancro. Il principale prodotto candidato dell'azienda è la belapectina (GR-MD-02), un inibitore della galectina-3, che si trova in uno studio clinico di Fase 2 su pazienti MASH con fibrosi avanzata e in un secondo studio clinico di Fase 2b su pazienti MASH con cirrosi compensata e ipertensione portale. L'azienda ha una joint venture con SBH Sciences, Inc. per la ricerca e lo sviluppo di piccole molecole organiche inibitrici della galectina-3 per somministrazione orale.

Galectin Therapeutics Inc. Riepilogo dei fondamenti

Come si confrontano gli utili e i ricavi di Galectin Therapeutics con la sua capitalizzazione di mercato?
GALT statistiche fondamentali
Capitalizzazione di mercatoUS$136.92m
Utili (TTM)-US$26.38m
Ricavi(TTM)n/a
0.0x
Rapporto P/S
-5.5x
Rapporto P/E

GALT è sopravvalutato?

Vedi Fair Value e analisi di valutazione

Utili e ricavi

Statistiche chiave sulla redditività dall'ultima relazione sugli utili (TTM)
GALT Conto economico (TTM)
RicaviUS$0
Costo del fatturatoUS$0
Profitto lordoUS$0
Altre speseUS$26.38m
Utili-US$26.38m

Ultimi utili riportati

Mar 31, 2026

Prossima data di guadagno

n/a

Utile per azione (EPS)-0.40
Margine lordo0.00%
Margine di profitto netto0.00%
Rapporto debito/patrimonio netto-104.2%

Come si è comportato GALT nel lungo periodo?

Vedi performance storica e confronto

Analisi aziendale e situazione dei dati finanziari

DatiUltimo aggiornamento (ora UTC)
Analisi dell'azienda2026/05/20 00:40
Prezzo dell'azione a fine giornata2026/05/20 00:00
Utili2026/03/31
Utili annuali2025/12/31

Fonti dei dati

I dati utilizzati nella nostra analisi aziendale provengono da S&P Global Market Intelligence LLC. I seguenti dati sono utilizzati nel nostro modello di analisi per generare questo report. I dati sono normalizzati, il che può comportare un ritardo nella disponibilità della fonte.

PacchettoDatiTempisticaEsempio Fonte USA *
Dati finanziari della società10 anni
  • Conto economico
  • Rendiconto finanziario
  • Bilancio
Stime di consenso degli analisti+3 anni
  • Previsioni finanziarie
  • Obiettivi di prezzo degli analisti
Prezzi di mercato30 anni
  • Prezzi delle azioni
  • Dividendi, scissioni e azioni
Proprietà10 anni
  • Top azionisti
  • Insider trading
Gestione10 anni
  • Team di leadership
  • Consiglio di amministrazione
Sviluppi principali10 anni
  • Annunci aziendali

* Esempio per i titoli statunitensi, per i titoli non statunitensi si utilizzano forme e fonti normative equivalenti.

Se non specificato, tutti i dati finanziari si basano su un periodo annuale ma vengono aggiornati trimestralmente. Si tratta dei cosiddetti dati TTM (Trailing Twelve Month) o LTM (Last Twelve Month). Per saperne di più.

Modello di analisi e Snowflake

I dettagli del modello di analisi utilizzato per generare questo report sono disponibili sulla nostra pagina Github; abbiamo anche guide su come utilizzare i nostri report e tutorial su Youtube.

Scoprite il team di livello mondiale che ha progettato e realizzato il modello di analisi Simply Wall St.

Metriche di settore e industriali

Le nostre metriche di settore e di sezione sono calcolate ogni 6 ore da Simply Wall St; i dettagli del nostro processo sono disponibili su Github.

Fonti analitiche

Galectin Therapeutics Inc. è coperta da 5 analisti. 1 di questi analisti ha fornito le stime di fatturato o di utile utilizzate come input per il nostro report. Le stime degli analisti vengono aggiornate nel corso della giornata.

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