Chloroarenes

BIOLASE and EdgeEndo Announce Plans to Develop New EdgePRO Laser-Assisted Microfluidic Irrigation Device for Endodontists

Retrieved on: 
Tuesday, April 20, 2021

This new Microfluidic Irrigation device is being developed to offer a solution for endodontists seeking more from their current cleaning and disinfection techniques, such as sodium hypochlorite, ethylenediaminetetraacetic acid, chlorhexidine or 2-in-1 or 3-in-1 irrigation solutions.

Key Points: 
  • This new Microfluidic Irrigation device is being developed to offer a solution for endodontists seeking more from their current cleaning and disinfection techniques, such as sodium hypochlorite, ethylenediaminetetraacetic acid, chlorhexidine or 2-in-1 or 3-in-1 irrigation solutions.
  • BIOLASE anticipates submitting a premarket notification (510(k)) to the Food and Drug Administration for the co-developed device in the second quarter of 2021.
  • This announcement comes on the heels of the recently developed Waterlase Endo Academy , open to all Waterlase endodontists.
  • Juric IB, Plecko V, Anic I. Antimicrobial Efficacy of Er,Cr:YSGG Laser-Activated Irrigation Compared with Passive Ultrasonic Irrigation and RinsEndo((R)) Against Intracanal Enterococcus faecalis.

Neurelis Announces Five Poster Presentations for the Annual Meeting of the American Academy Of Neurology

Retrieved on: 
Monday, April 19, 2021

In addition, the data shows that patients reported feeling like their usual self within two hours after VALTOCO administration.

Key Points: 
  • In addition, the data shows that patients reported feeling like their usual self within two hours after VALTOCO administration.
  • To be able to continue on with your day is very meaningful for patients with seizure clusters.
  • In a long-term, open-label, repeat-dose clinical trial, the safety of VALTOCO was evaluated, and more than 4,000 seizures were treated.
  • Serious and fatal adverse reactions, including "gasping syndrome", can occur in neonates and low-birth-weight infants treated with benzyl alcohol-preserved drugs, including VALTOCO.

Arcus Biosciences Presents Updated Data for Etrumadenant in Third-Line Metastatic Colorectal Cancer and New Data on its HIF-2α Program at the AACR 2021 Annual Meeting

Retrieved on: 
Saturday, April 10, 2021

Efficacy Results (n=22 efficacy-evaluable 3L+ patients as of the DCO of Feb. 26, 2021)

Key Points: 
  • Efficacy Results (n=22 efficacy-evaluable 3L+ patients as of the DCO of Feb. 26, 2021)
    Median progression-free survival (PFS) of 4.2 months.
  • Reported data for current standard-of-care (SOC) therapies have shown a median PFS of 2.0 and 1.9 months for trifluridine-tipiracil and regorafenib, respectively3,4.
  • Reported data for trifluridine-tipiracil and regorafenib have shown a median OS of 7.1 and 6.4 months, respectively3,4.
  • Few options exist today to treat third-line colorectal cancer, and these therapies are associated with significant toxicity and limited efficacy.

Cosmos Holdings Launches Mosept-Oral Antiseptic Spray Designed to be Effective Against Bacteria and Certain Viral Pathogens

Retrieved on: 
Thursday, April 8, 2021

The Company has also started the registration process for Mosept-Oral for the UK with the submission of the documentation for the formulation.

Key Points: 
  • The Company has also started the registration process for Mosept-Oral for the UK with the submission of the documentation for the formulation.
  • Initial target countries are the United Kingdom, Germany, the Netherlands, France, Italy, Spain, Cyprus, Canada and the Middle East.
  • The mouth spray was formulated, designed and developed entirely by the Cosmos Holdings research and development team.
  • Chlorhexidine is a bisbiguanide antiseptic and disinfectant which is bactericidal or bacteriostatic against a wide range of Gram-positive and Gram-negative bacteria and inhibits the proliferation of certain viruses and fungi.

Hyundai Bioscience leads in the repurposing of Niclosamide

Retrieved on: 
Thursday, April 8, 2021

CNPharm also filed international patent applications on this DDS technology for repurposing Niclosamide as COVID-19 treatment.

Key Points: 
  • CNPharm also filed international patent applications on this DDS technology for repurposing Niclosamide as COVID-19 treatment.
  • This means that the international pharmaceutical community has recognized that CNPharm, the parent company of Hyundai Bioscience, is leading the way to repurpose the anthelmintic drug.
  • An official at Hyundai Bioscience stated that this is the first time that Niclosamide's bioavailability improvement for drug repurposing has been published in an international journal.
  • Based on CNPharm's original technology, Hyundai Bioscience has dramatically improved the absorption rate and half-life of Niclosamide last year, developing CP-COV03, an oral treatment for COVID-19.

Evoke Pharma Receives Notice of Allowance from United States Patent and Trademark Office for a Method of Use Patent with Claims Covering Gimoti®

Retrieved on: 
Tuesday, April 6, 2021

When granted, the patent will cover methods of use for nasal delivery of metoclopramide for the treatment of gastroparesis.

Key Points: 
  • When granted, the patent will cover methods of use for nasal delivery of metoclopramide for the treatment of gastroparesis.
  • The patent, entitled Nasal Formulations of Metoclopramide, carries a patent term to at least 2029.
  • Gimoti is Evokes nasal spray product for the relief of symptoms in acute and recurrent diabetic gastroparesis.
  • This new patent covers Gimoti for gastroparesis and will be listable in FDAs Orange Book.

AzurRx BioPharma Initiates Phase 2 Clinical Trial of Niclosamide for the Treatment of COVID-19 Gastrointestinal Infections

Retrieved on: 
Tuesday, April 6, 2021

These long term observation data could indicate that niclosamide treatment has the potential to improve long haul COVID-19 symptoms.

Key Points: 
  • These long term observation data could indicate that niclosamide treatment has the potential to improve long haul COVID-19 symptoms.
  • We look forward to testing this hypothesis in the RESERVOIR Phase 2 trial and reporting topline data from the trial in early 2022.
  • FW-1022 is a niclosamide based small molecule which the Companys clinical trials may establish has anti-viral activity that is effective for the treatment of SARS-CoV-2 (COVID-19) gastrointestinal infections.
  • AzurRx BioPharma, Inc. (NASDAQ: AZRX) is a clinical stage biopharmaceutical company specializing in the development of targeted, non-systemic therapies for gastrointestinal (GI) diseases.

New England Journal of Medicine Publishes Results of the PULSAR Phase 2 Trial of Sotatercept in Patients with Pulmonary Arterial Hypertension

Retrieved on: 
Thursday, April 1, 2021

This is a result that suggests that sotatercept could bring an important new mechanistic approach to the treatment of patients with PAH.

Key Points: 
  • This is a result that suggests that sotatercept could bring an important new mechanistic approach to the treatment of patients with PAH.
  • The PULSAR publication marks the third time that trial results of an Acceleron-discovered therapy have been published in the New England Journal of Medicine in the past 15 months.
  • The PULSAR Phase 2 trial is a randomized, double-blind, placebo-controlled study designed to evaluate the efficacy and safety of sotatercept in patients with PAH.
  • In pulmonary, Acceleron is developing sotatercept for the treatment of pulmonary arterial hypertension (PAH), having reported positive topline results of the PULSAR Phase 2 trial.

DGAP-News: Newron announces results of explanatory studies with evenamide in healthy volunteers and patients with schizophrenia

Retrieved on: 
Thursday, April 1, 2021

These results strongly suggest that evenamide does not increase a patient's risk of QTc prolongation and arrhythmias, a risk generally associated with antipsychotics.

Key Points: 
  • These results strongly suggest that evenamide does not increase a patient's risk of QTc prolongation and arrhythmias, a risk generally associated with antipsychotics.
  • No patient on evenamide discontinued from the study due to adverse events, and there were no significant adverse events relating to evenamide.
  • Evenamide has the potential to be first add-on therapy for the treatment of patients with positive symptoms of schizophrenia.
  • Newron is also developing evenamide as the potential first add-on therapy for the treatment of patients with positive symptoms of schizophrenia.

Apotex Corp. Issues Voluntary Nationwide Recall of Guanfacine Extended-Release Tablets 2mg due to trace amounts of Quetiapine Fumarate

Retrieved on: 
Wednesday, March 31, 2021

The three (3) affected lots of Guanfacine extended-release tablets were distributed by Apotex nationwide in the USA to Wholesalers, Distributors, Warehousing Chains, Independent Retail Pharmacy and Retail Buying Group.

Key Points: 
  • The three (3) affected lots of Guanfacine extended-release tablets were distributed by Apotex nationwide in the USA to Wholesalers, Distributors, Warehousing Chains, Independent Retail Pharmacy and Retail Buying Group.
  • Patients who have received either of the three impacted lots of Guanfacine Extended-Release Tablets or have questions regarding this recall should contact their pharmacy.
  • Wholesalers, Distributors, Warehousing Chains, Independent Retail Pharmacy and Retail Buying Group should return the recalled product to the place of purchase.
  • Consumers with questions regarding this recall can contact Apotex Corp. by phone at 1-800-706-5575 (8:30am 5:00pm, EST Monday thru Friday) or email address [email protected] .