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ELOXX PHARMACEUTICALS INC - ELOX STOCK NEWS

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Eloxx Pharmaceuticals, Inc. (NASDAQ: ELOX) is a clinical-stage biopharmaceutical company focused on the development of novel RNA-modulating drug candidates designed to treat rare and ultra-rare premature stop codon diseases. Premature stop codons are genetic mutations that disrupt protein synthesis, leading to severe genetic disorders. With over 1,800 identified rare diseases caused by these mutations, Eloxx is at the forefront of innovative genetic therapies.

The company's lead product candidate, ELX-02, is a small molecule drug designed to restore production of full-length functional proteins. Currently in Phase 2 clinical development, ELX-02 has shown promise in treating Alport syndrome, a genetic disorder characterized by kidney disease, hearing loss, and eye abnormalities.

Recent advancements include confirmation of ELX-02's disease-modifying potential in Alport syndrome, with positive results from patient biopsies in clinical trials. Eloxx has also submitted an Investigational New Drug (IND) application to the U.S. FDA for ELX-02, aiming to include U.S.-based sites in its pivotal trials.

Additionally, Eloxx is developing ZKN-013, a TURBO-ZM™ based molecule for treating recessive dystrophic epidermolysis bullosa (RDEB) and other genetic conditions. The company has initiated strategic partnerships and aims to begin patient dosing by the end of 2023.

Financially, Eloxx reported a net loss of $3.6 million for Q3 2023 but has shown a decrease in overall R&D and administrative expenses compared to the previous year. The company is focused on improving its liquidity position and raising additional capital to fund operations through 2023 and beyond.

Eloxx continues to leverage its TURBO-ZM™ chemistry platform to develop novel Ribosome Modulating Agents (RMAs) and maintain its commitment to addressing the unmet medical needs of patients with rare genetic disorders. For the latest updates and detailed information, visit www.eloxxpharma.com.

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Eloxx Pharmaceuticals (NASDAQ: ELOX) announced topline results from its Phase 2 trial of ELX-02 combined with ivacaftor for treating Class 1 cystic fibrosis patients. The trial showed that while ELX-02 was well tolerated with no serious adverse events, it failed to achieve statistical significance for key efficacy endpoints, including sweat chloride concentration and forced expiratory volume. Notably, there was evidence of activity, particularly in patients with higher baseline sweat chloride levels. Eloxx plans to collaborate with the CF Foundation for future steps and will initiate a proof-of-concept trial for Alport syndrome.

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Eloxx Pharmaceuticals (NASDAQ: ELOX) reported significant advancements in their clinical pipeline, targeting rare diseases. The company anticipates topline data from Phase 2 trials in cystic fibrosis and Alport syndrome by Q3 2022. Additionally, they are set to file IND applications for ELX-02 and ZKN-013 targeting various conditions by Q4 2022. Financially, Eloxx experienced a net loss of $10.6 million for Q2 2022, an improvement from $36.1 million in the same quarter last year. Cash reserves are projected to sustain operations through Q4 2023.

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Eloxx Pharmaceuticals (NASDAQ: ELOX) announced the appointment of Lindsay Androski, JD, MBA, to its board of directors, alongside her role in the Audit and Compensation Committees. This follows the departure of several board members including Gadi Veinrib and Ran Nussbaum. Androski, an experienced biotech executive from Roivant Social Ventures, aims to enhance Eloxx's focus on genetic therapies for rare diseases. The board restructuring supports the company's strategic transformation initiated with the Zikani acquisition in April 2021.

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Eloxx Pharmaceuticals (NASDAQ: ELOX) announced a funding award of up to $15.9 million from the Cystic Fibrosis Foundation for its ELX-02 clinical program targeting Class 1 cystic fibrosis. Phase 2 trial results are expected by mid-2022. The company also plans to expand ELX-02's application to Alport syndrome, initiating a Phase 2 trial in late 2022. Financially, Eloxx incurred a net loss of $11.6 million for Q1 2022, with R&D expenses rising to $7.9 million. Cash reserves are anticipated to last until mid-2023.

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Eloxx Pharmaceuticals (ELOX) announced a funding award of up to $15.9 million from the Cystic Fibrosis Foundation for its ELX-02 clinical development in treating cystic fibrosis (CF). The Phase 2 trial results are expected in mid-2022. The company is extending its pipeline to include Alport syndrome and plans to start proof-of-concept trials later in 2022. In preclinical studies, ZKN-013 showed promising results for treating recessive dystrophic epidermolysis bullosa and familial adenomatous polyposis. Financial results reveal a net loss of $12.1 million for Q4 2021.

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Eloxx Pharmaceuticals (ELOX) has expanded its ELX-02 program to target Alport syndrome, a rare kidney disease caused by mutations in collagen genes. The initiation of a proof-of-concept clinical trial is expected in the second half of 2022, assessing up to eight patients with nonsense mutations. ELX-02 has shown promise in preclinical studies, demonstrating significant readthrough in COL4A5 mutations. Topline results from the trial are anticipated in the first half of 2023, marking a potential breakthrough in treating this underserved patient population.

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Eloxx Pharmaceuticals (NASDAQ: ELOX) announced a Therapeutic Development Award of up to $15.9 million from the Cystic Fibrosis Foundation to support its ELX-02 clinical program. This funding builds on prior support and is contingent on achieving specific clinical milestones. The Phase 2 trial combines ELX-02 with ivacaftor, targeting Class 1 CF patients with nonsense mutations, a group with no current treatment options. Management expects topline results by mid-2022, along with a cash runway extension into Q2 2023. ELX-02 has Fast Track and Orphan Drug designations from the FDA.

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ELX-02, administered at 1.5mg/kg/day, showed a significant mean reduction of 5.4mmol/L in sweat chloride levels, indicating potential CFTR activity restoration in cystic fibrosis patients. The results support moving ELX-02 into Phase 3 trials. The FDA has granted Fast Track and Orphan Drug Designations for ELX-02. Additionally, the company has started a Phase 2 expansion for ELX-02 combined with ivacaftor, with results anticipated by mid-2022. Eloxx aims to explore inhaled delivery of ELX-02 to enhance efficacy.

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Eloxx Pharmaceuticals (NASDAQ: ELOX) reported its Q3 2021 results, posting a net loss of $9.9 million, up from $6.6 million in Q3 2020. The company is progressing with its Phase 2 ELX-02 clinical trials for cystic fibrosis, expecting data in late 2021. ELX-02 received FDA Fast Track designation, highlighting its potential for serious medical needs. Eloxx entered a debt facility with Hercules Capital for up to $30 million, drawing an initial $12.5 million. As of September 30, 2021, cash reserves stood at $52.4 million, projected to last through Q1 2023.

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Eloxx Pharmaceuticals, Inc. (Nasdaq: ELOX) will host an Investor and Analyst call on October 12, 2021, featuring Dr. Eitan Kerem, a prominent cystic fibrosis (CF) expert. The call aims to provide updates on the company’s CF programs as data from ongoing Phase 2 trials are expected in Q4 2021. The call is scheduled for 10:00 a.m. ET, with both domestic and international dial-in options available. The event will be webcast live and accessible on the company's website, with a replay available for 30 days afterwards.

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FAQ

What is the current stock price of ELOXX PHARMACEUTICALS (ELOX)?

The current stock price of ELOXX PHARMACEUTICALS (ELOX) is $0.000001 as of December 20, 2024.

What is the market cap of ELOXX PHARMACEUTICALS (ELOX)?

The market cap of ELOXX PHARMACEUTICALS (ELOX) is approximately 314.0.

What is Eloxx Pharmaceuticals' primary focus?

Eloxx Pharmaceuticals focuses on developing RNA-modulating drug candidates to treat rare and ultra-rare premature stop codon diseases.

What is ELX-02?

ELX-02 is Eloxx's lead product candidate, a small molecule drug designed to restore production of full-length functional proteins, currently in Phase 2 clinical development for treating Alport syndrome.

What is the significance of premature stop codons?

Premature stop codons are genetic mutations that disrupt protein synthesis, leading to severe genetic disorders. Eloxx targets these mutations to restore protein production.

What are the recent advancements with ELX-02?

ELX-02 has shown disease-modifying potential in clinical trials for Alport syndrome, with positive results in patient biopsies and an IND submission to the FDA for further trials.

What is ZKN-013?

ZKN-013 is a TURBO-ZM™ based molecule under development by Eloxx for treating recessive dystrophic epidermolysis bullosa (RDEB) and other genetic conditions.

How is Eloxx Pharmaceuticals performing financially?

Eloxx reported a net loss of $3.6 million for Q3 2023, with decreased R&D and administrative expenses compared to the previous year. The company is focused on improving liquidity and raising additional capital.

What is the TURBO-ZM™ platform?

The TURBO-ZM™ platform is Eloxx's innovative chemistry technology platform used to develop novel Ribosome Modulating Agents (RMAs) for treating genetic disorders.

What are the challenges Eloxx Pharmaceuticals is facing?

Eloxx is focused on improving its liquidity position, raising additional capital, and maintaining compliance with Nasdaq listing requirements.

What are Eloxx's future plans?

Eloxx plans to advance ELX-02 into pivotal trials for Alport syndrome, initiate clinical studies for ZKN-013, and continue leveraging their TURBO-ZM™ platform for new therapies.

Where can I find more information about Eloxx Pharmaceuticals?

For more information, visit Eloxx Pharmaceuticals' official website at www.eloxxpharma.com.

ELOXX PHARMACEUTICALS INC

Nasdaq:ELOX

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