IGC Pharma Announces Research Demonstrating New Molecule IGC-1C Targets Tau Protein in Alzheimer's Disease

Rhea-AI Summary

IGC Pharma (NYSE American: IGC) has announced promising preclinical research on IGC-1C, a novel small-molecule modulator. The findings reveal that IGC-1C targets tau protein phase separation, offering new possibilities for treating neurodegenerative diseases. Additionally, IGC-1C has been identified as a potential GLP-1 receptor agonist, showing promise for weight loss treatments and presenting a unique strategy to combat Alzheimer's disease.

Key points:

• IGC-1C exhibits a dissociation constant (Kd) of 3.95 ± 0.32 μM with tau, indicating strong binding affinity
• The molecule effectively inhibits tau condensates and prevents their transition into toxic fibrils
• IGC-1C's dual action targets both tau and GLP-1 receptors, potentially addressing multiple pathways in Alzheimer's and metabolic disorders
• The company aims to advance IGC-1C through future clinical trials

Positive

• IGC-1C demonstrates strong binding affinity with tau protein, potentially addressing a key hallmark of Alzheimer's disease
• The molecule shows potential as a GLP-1 receptor agonist, expanding its therapeutic applications to weight loss and metabolic disorders
• IGC-1C's dual-action mechanism could offer a comprehensive approach to treating Alzheimer's disease and related conditions

Negative

• The research is still in preclinical stages, requiring further clinical trials to prove efficacy and safety in humans
• There is no guarantee that the promising preclinical results will translate to successful clinical outcomes

Medical Research Analyst

The preclinical research on IGC-1C presents a potentially significant breakthrough in Alzheimer's disease treatment. The molecule's dual action, targeting both tau protein and GLP-1 receptors, offers a novel multi-pathway approach. With a dissociation constant (Kd) of 3.95 ± 0.32 μM, IGC-1C demonstrates strong binding affinity to tau, important for inhibiting the formation of neurofibrillary tangles.

The ability of IGC-1C to disrupt tau condensates and prevent their transition into toxic fibrils is particularly promising. This mechanism could potentially slow down Alzheimer's progression, addressing a key pathological hallmark of the disease. Moreover, its potential as a GLP-1 receptor agonist opens up possibilities for treating metabolic disorders and obesity, which are often comorbid with Alzheimer's.

However, it's important to note that these are early-stage findings. The transition from preclinical to clinical studies often reveals unforeseen challenges. Investors should monitor future clinical trials to assess IGC-1C's efficacy and safety in humans.

Financial Analyst

This announcement could have a positive impact on IGC Pharma's stock. The company's focus on developing a multi-pathway treatment for Alzheimer's and metabolic disorders positions it in high-value pharmaceutical markets. The global Alzheimer's drug market is projected to reach $5.66 billion by 2024, while the GLP-1 receptor agonist market for diabetes and obesity is expected to exceed $20 billion by 2025.

However, investors should exercise caution. Drug development is a long, costly process with high failure rates. IGC Pharma will need substantial funding to advance IGC-1C through clinical trials. The company's financial position and burn rate will be important factors to watch. Additionally, competition in both Alzheimer's and metabolic disorder treatments is intense, with several big pharma players involved.

While the news is promising, it's important to remember that many preclinical candidates don't make it to market. Investors should consider this announcement as a long-term potential rather than an immediate value driver.

Neuroscience Expert

The dual-action mechanism of IGC-1C is intriguing from a neuroscientific perspective. Targeting tau protein aggregation addresses a critical aspect of Alzheimer's pathology that has been challenging to tackle. The molecule's ability to inhibit zinc-induced liquid-liquid phase separation (LLPS) of tau is particularly noteworthy, as it could prevent the formation of toxic tau fibrils at an early stage.

The potential GLP-1 receptor agonist activity adds another layer of neuroprotection. GLP-1 receptor activation has shown promise in reducing oxidative stress, inflammation and promoting Aβ clearance in Alzheimer's models. This multi-faceted approach could prove more effective than single-target therapies.

However, it's important to note that the complexity of Alzheimer's disease has thwarted many promising candidates in the past. The transition from in vitro studies to in vivo efficacy is a significant hurdle. Future animal studies and early-phase clinical trials will be critical in validating IGC-1C's potential as a transformative therapy for Alzheimer's and metabolic disorders.

IGC-1C Targets Tau Protein and GLP-1 Receptor, Offering a Multi-Pathway Approach to Neurodegenerative and Metabolic Disease Treatment

POTOMAC, Md.--(BUSINESS WIRE)-- IGC Pharma, Inc. (NYSE American: IGC) ("IGC Pharma" or the "Company") today announced preclinical research demonstrating the therapeutic potential of IGC-1C, a novel small-molecule modulator. The findings show that IGC-1C targets tau protein phase separation, presenting new opportunities for addressing multiple pathways in neurodegenerative disease.

Additionally, the Company previously announced that IGC-1C along with IGC-1A have been identified by the Company's Artificial Intelligence ("AI") model as potential GLP-1 receptor agonists, offering promise as candidates for weight loss treatments and presenting a unique strategy to combat Alzheimer's disease.

Preclinical investigations indicate that IGC-1C exhibits a dissociation constant (Kd) of 3.95 ± 0.32 μM with tau, demonstrating a robust binding affinity that supports its potential as a therapeutic agent. The Kd value reflects the strength of the interaction between IGC-1C and tau, and this high affinity reinforces IGC-1C's efficacy in modulating tau protein, which is involved in the formation of neurofibrillary tangles, a key hallmark of Alzheimer's disease.

IGC-1C, a cyclic dipeptide-based small-molecule modulator, represents a pioneering approach to addressing tau-related pathology. The in-vitro research shows that IGC-1C effectively inhibits tau condensates formed by zinc-induced liquid-liquid phase separation ("LLPS") and prevents their transition into toxic fibrils. By disrupting this phase separation and aggregation process, IGC-1C could, subject to more trials, halt the formation of tau tangles, offering a potential breakthrough in slowing Alzheimer's progression.

"Our discovery of IGC-1C's potential dual action, targeting both tau and GLP-1 receptors, marks a significant advancement in our Alzheimer's disease research and treatment," said Ram Mukunda, CEO of IGC Pharma. "This innovative approach aligns with our broader strategy to develop and leverage several assets in the metabolic disease space, aiming to improve treatment outcomes for Alzheimer's, metabolic disorders and obesity. By addressing the emerging focus on tau tangles and incorporating GLP-1 receptor modulation, IGC-1C positions itself at the forefront of developing transformative therapies, providing a comprehensive strategy for slowing progression and improving patient outcomes. We are committed to advancing our molecules through future clinical trials, fully realizing its potential to deliver transformative therapies and drive substantial value for our shareholders."

Tau pathology in Alzheimer's is driven by hyperphosphorylation, where tau proteins form neurotoxic tangles strongly correlated with significant cognitive decline, memory loss, and other debilitating symptoms. Neurofibrillary tangles typically appear in the later stages of Alzheimer's disease and are a vital indicator of the disease's progression.

In addition to its impact on tau pathology, IGC-1C has been identified as a potential GLP-1 receptor agonist. GLP-1 (glucagon-like peptide-1) is a hormone with receptors throughout the brain, including areas affected by Alzheimer's. Research indicates that GLP-1 has been shown to be neuroprotective against Aβ toxicity by reducing oxidative stress and inflammation, increasing Aβ clearance, improving insulin signaling, and promoting neurogenesis. This dual mechanism positions IGC-1C as a promising candidate for treating weight loss, and neurodegenerative and metabolic disorders, although there can be no assurance thereof.

About IGC Pharma (dba IGC):

IGC Pharma is an AI-powered, clinical-stage biotechnology company focused on developing innovative treatments for Alzheimer's disease and transforming patient care with fast-acting, safe, and effective solutions. Our portfolio includes the TGR family, including TGR-63, which targets amyloid plaques, a hallmark of Alzheimer's. The IGC-C and IGC-M platforms are advancing in preclinical studies, focusing on metabolic disorders, tau proteins, early plaque formation, and multiple disease hallmarks. Our lead therapeutic candidate, IGC-AD1, is a cannabinoid-based treatment currently in a Phase 2 trial for agitation in dementia associated with Alzheimer's (clinicaltrials.gov, NCT05543681). Interim data for IGC-AD1 demonstrated that it has the potential to transform patient care by offering faster-acting and more effective relief compared to traditional medications. Additionally, our AI models are designed to predict potential biomarkers for the early detection of Alzheimer's, optimize clinical trials, and predict receptor affinity, among others. With 28 patent filings and a commitment to innovation, IGC Pharma is dedicated to advancing pharmaceutical treatments and improving the lives of those affected by Alzheimer's and related conditions.

Forward-looking Statements

This press release contains forward-looking statements. These forward-looking statements are based largely on IGC Pharma's expectations and are subject to several risks and uncertainties, certain of which are beyond IGC Pharma's control. Actual results could differ materially from these forward-looking statements as a result of, among other factors, the Company's failure or inability to commercialize one or more of the Company's products or technologies, including the products or formulations described in this release, or failure to obtain regulatory approval for the products or formulations, where required, or government regulations affecting AI or the AI algorithms not working as intended or producing accurate predictions; general economic conditions that are less favorable than expected; the FDA's general position regarding cannabis- and hemp-based products; and other factors, many of which are discussed in IGC Pharma's U.S. Securities and Exchange Commission ("SEC") filings. IGC incorporates by reference its Annual Report on Form 10-K filed with the SEC on June 24, 2024, and on Form 10-Q filed with the SEC on August 7, 2024, as if fully incorporated and restated herein. Considering these risks and uncertainties, there can be no assurance that the forward-looking information contained in this release will occur.

View source version on businesswire.com: https://www.businesswire.com/news/home/20240822040435/en/

IMS Investor Relations

Rosalyn Christian / Walter Frank

igc@imsinvestorrelations.com

(203) 972-9200

Source: IGC Pharma, Inc.

FAQ

What is IGC-1C and how does it target Alzheimer's disease?

IGC-1C is a novel small-molecule modulator developed by IGC Pharma. It targets tau protein phase separation, which is involved in the formation of neurofibrillary tangles, a key hallmark of Alzheimer's disease. IGC-1C also shows potential as a GLP-1 receptor agonist, offering a dual-action approach to treating Alzheimer's.

What are the potential applications of IGC-1C beyond Alzheimer's disease?

IGC-1C shows promise as a GLP-1 receptor agonist, which could make it a potential candidate for weight loss treatments and addressing metabolic disorders. This dual mechanism positions IGC-1C as a versatile therapeutic option for multiple conditions.

What is the significance of IGC-1C's binding affinity with tau protein?

IGC-1C exhibits a dissociation constant (Kd) of 3.95 ± 0.32 μM with tau, demonstrating a robust binding affinity. This strong interaction supports IGC-1C's potential efficacy in modulating tau protein, which is important in addressing the formation of neurofibrillary tangles in Alzheimer's disease.

How does IGC Pharma (IGC) plan to advance the development of IGC-1C?

IGC Pharma aims to advance IGC-1C through future clinical trials to fully realize its potential as a transformative therapy for Alzheimer's disease, metabolic disorders, and obesity. The company is committed to developing and leveraging several assets in the metabolic disease space to improve treatment outcomes.