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Prothena Corporation plc Ordinary Shares - PRTA STOCK NEWS

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Prothena Corporation plc (NASDAQ: PRTA) is a leading biotechnology company dedicated to the discovery, development, and commercialization of novel protein immunotherapies. These therapies aim to treat diseases involving amyloid or cell adhesion. Prothena's core business focuses on developing therapeutic monoclonal antibodies that target disease-causing proteins.

The company's investigational therapeutics are designed to address various serious conditions. Prothena's product candidates target a range of indications, including:

  • Amyloid Light-chain (AL) amyloidosis (NEOD001): Currently in a global Phase 3 registration clinical trial, known as the VITAL Amyloidosis Study. Additionally, there is an ongoing Phase 1/2 trial.
  • Parkinson’s disease and other synucleinopathies (PRX002): Undergoing a Phase 1 multiple ascending dose clinical trial.
  • Psoriasis and other inflammatory diseases (PRX003): In a Phase 1 single ascending dose clinical trial.

Prothena’s lead program, NEOD001, is aimed at treating AL amyloidosis, a serious condition that affects the organs. PRX002 and PRX003 are also significant as they target critical unmet needs in neurodegenerative and inflammatory diseases.

The company’s strategy is underpinned by a robust scientific approach and a pipeline of promising candidates. Prothena is led by an elite team with a proven track record in biotechnology and pharmaceuticals, working tirelessly to bring breakthrough therapies to market.

Financially, Prothena is in a strong position, bolstered by strategic partnerships and a focus on high-potential therapeutic areas. The company continues to advance its clinical programs while exploring new avenues for growth and innovation.

Latest News: Stay updated with the most recent developments and updates from Prothena Corporation plc.

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Prothena Corporation announced significant findings from the VITAL study, highlighting birtamimab's survival benefit in Mayo Stage IV AL amyloidosis patients, achieving a hazard ratio of 0.413 (p=0.025) over 9 months. Following these results, Prothena has entered a Special Protocol Assessment (SPA) agreement with the FDA for a confirmatory Phase 3 study, AFFIRM-AL, set to begin in mid-2021, focusing on all-cause mortality (p<0.10). The total enrollment will target about 150 patients and will assess secondary endpoints related to quality of life.

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Prothena Corporation plc (NASDAQ:PRTA) announced positive Phase 1 results for PRX004, an anti-amyloid immunotherapy targeting ATTR amyloidosis. All 7 evaluable patients exhibited a +1.29 point change in Neuropathy Impairment Score (NIS) after 9 months, significantly better than the expected +9.2 points from untreated patients. Three patients reported improvement in neuropathy, with a mean change of –3.33 points. Additionally, cardiac function improved in all evaluable patients. PRX004 demonstrated a favorable safety profile, with no serious adverse events reported.

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Prothena Corporation (NASDAQ:PRTA) announced the grant of options to purchase 90,000 ordinary shares to two new employees. The options have an exercise price of $11.00, reflecting the closing price as of December 1, 2020. These options will vest over four years, with 25% vesting after one year and the remaining shares vesting monthly thereafter. This incentive aims to encourage new talent to join Prothena, a company specializing in therapeutics for neurodegenerative diseases and amyloid-related conditions.

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Prothena Corporation reported a net loss of $30.6 million for Q3 2020, compared to $19.4 million in Q3 2019. The company has $317.2 million in cash as of September 30, 2020, ensuring funding for ongoing R&D initiatives. Key highlights include the presentation of positive Phase 2 results for prasinezumab in Parkinson's disease, showing a 35% reduction in motor decline, and its advancement into a late-stage study. The company plans to earn a $60 million milestone payment upon dosing the first patient in this study.

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Prothena Corporation presents preclinical data on its Alzheimer’s disease portfolio at CTAD 2020, showcasing next-generation anti-Aβ antibodies and a multi-immunogen Aβ-tau vaccine. The anti-Aβ antibodies, designed for subcutaneous administration, exhibit 11-fold greater binding strength to amyloid compared to aducanumab, enhancing patient access. The dual-target vaccine aims to tackle both Aβ and tau pathologies, generating balanced immune responses. Prothena's innovative approaches address significant challenges in patient treatment accessibility and represent a potential step forward in Alzheimer’s therapeutics.

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Prothena Corporation plc (NASDAQ:PRTA) will disclose its third quarter and first nine months of 2020 financial results on November 4, after U.S. market close. The company specializes in protein dysregulation and has an extensive pipeline targeting neurodegenerative and rare amyloid diseases. Notably, it collaborates with Roche on prasinezumab for Parkinson’s and with Bristol-Myers Squibb for Alzheimer’s and related conditions. Prothena will not hold a conference call for this earnings release.

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Prothena Corporation has announced that its anti-alpha-synuclein antibody, prasinezumab, will progress to a Phase 2b study focusing on patients with early Parkinson's disease, following positive results from the PASADENA study. This trial is set to evaluate efficacy further and is expected to initiate in 2021. Prothena will receive a $60 million milestone payment upon dosing the first patient. The ongoing research aims to address the underlying causes of Parkinson's, impacting a significant number of individuals globally, as current treatments only manage symptoms.

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Prothena Corporation (NASDAQ: PRTA) announced the hiring of two new employees, granting stock options to purchase 50,000 shares at an exercise price of $10.31 each. The options will vest over four years, with 25% vesting after one year and the remainder monthly thereafter. This move is part of Prothena’s 2020 Employment Inducement Incentive Plan aimed at attracting talent in the field of neurodegenerative diseases. Prothena focuses on investigational therapeutics for amyloid diseases and has partnered programs targeting various neurological conditions.

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Prothena Corporation plc (NASDAQ: PRTA) will hold an investor webcast today at 1:30 PM ET following Roche's presentation of the Phase 2 PASADENA study results at the MDS Virtual Congress 2020. The webcast will review the findings from this study, which focuses on therapeutics for neurodegenerative diseases. Investors can access the presentation via Prothena's website, with a replay available for 90 days. Prothena specializes in developing treatments for conditions such as Parkinson's disease and amyloidosis, leveraging its expertise in protein dysregulation.

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Prothena Corporation (NASDAQ:PRTA) announced encouraging results from the Phase 2 PASADENA study of prasinezumab, an anti-alpha-synuclein antibody aimed at early Parkinson's disease. Although the primary endpoint was not met, significant efficacy signals were observed, including a 35% reduction in motor function decline compared to placebo after one year. The drug also delayed clinically meaningful worsening of motor progression. These results support further clinical development of prasinezumab as a potential disease-modifying therapy, with an investor webcast scheduled for September 15, 2020.

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FAQ

What is the current stock price of Prothena Corporation plc Ordinary Shares (PRTA)?

The current stock price of Prothena Corporation plc Ordinary Shares (PRTA) is $11.95 as of December 18, 2024.

What is the market cap of Prothena Corporation plc Ordinary Shares (PRTA)?

The market cap of Prothena Corporation plc Ordinary Shares (PRTA) is approximately 634.5M.

What is the primary focus of Prothena Corporation plc?

Prothena focuses on the discovery, development, and commercialization of novel protein immunotherapies for diseases involving amyloid or cell adhesion.

What are the main indications Prothena's products target?

Prothena's product candidates target AL amyloidosis (NEOD001), Parkinson’s disease (PRX002), and inflammatory diseases like psoriasis (PRX003).

What is NEOD001?

NEOD001 is Prothena's lead program aimed at treating AL amyloidosis. It is currently in a global Phase 3 registration clinical trial, the VITAL Amyloidosis Study.

Which clinical trials are PRX002 and PRX003 undergoing?

PRX002 is in a Phase 1 multiple ascending dose clinical trial, while PRX003 is in a Phase 1 single ascending dose clinical trial.

What makes Prothena's approach unique?

Prothena's approach is unique due to its focus on monoclonal antibodies targeting disease-causing proteins, a robust scientific strategy, and a team with a proven track record.

How is Prothena financially positioned?

Prothena is financially strong, supported by strategic partnerships and a dedicated focus on high-potential therapeutic areas.

Who leads Prothena Corporation plc?

Prothena is led by an elite team with recognized expertise and a successful track record in biotechnology and pharmaceuticals.

What is the VITAL Amyloidosis Study?

The VITAL Amyloidosis Study is a global Phase 3 registration clinical trial for Prothena's lead program, NEOD001, aimed at treating AL amyloidosis.

How does Prothena contribute to treating Parkinson's disease?

Prothena is developing PRX002, a monoclonal antibody targeting synucleinopathies, including Parkinson’s disease, currently in a Phase 1 clinical trial.

What are the latest developments at Prothena Corporation plc?

For the latest news and updates on Prothena's clinical programs and strategic initiatives, visit their official website or news sections.

Prothena Corporation plc Ordinary Shares

Nasdaq:PRTA

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634.51M
46.57M
13.46%
96.98%
14.64%
Biotechnology
Pharmaceutical Preparations
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United States of America
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