Sound Pharmaceuticals to launch NIH-funded Covid-19 oral therapeutic trial

Sound Pharmaceuticals is all set to launch two Phase II clinical trials of an oral capsule, SPI-1005, for treating patients with moderate or severe Covid-19.

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Developed for various neurotologic, neuropsychiatric, and respiratory indications, SPI-1005 is a capsule with a small molecule called ebselen.

The latest development comes after Sound Pharmaceuticals received a Cooperative Grant award worth $3.1m from the US National Institutes of Health (NIH) unit National Center for Advancing Translational Sciences (NCATS) for evaluating SPI-1005.

 Sound Pharmaceuticals co-founder and CEO Dr Jonathan Kil said: “We are honoured to receive NIH funding for this novel therapeutic application of ebselen in Covid-19.

“To our knowledge, these are the first Phase II studies of an Mpro or PLpro inhibitor in moderate and severe Covid-19.”

 The two randomised, double-blind, placebo-controlled trials will enrol 120 subjects with moderate or severe Covid-19. They will receive SPI-1005 or placebo for seven or 14 days.

Furthermore, the company will assess whether SPI-1005 can enhance the body’s inflammatory and cellular immune response to Covid-19.

In a separate development, Moleculin Biotech and IQVIA Biotech are set to initiate potential clinical trials of the former’s drug, WP1122, for treating Covid-19.

UNION therapeutics’ Covid-19 candidates meet endpoints in trial

UNION therapeutics has reported that its Covid-19 candidates, inhaled and intranasal niclosamide (UNI91103 and UNI91104), showed a strong safety profile in a Phase I study, meeting the primary endpoints.

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UNI91103 and UNI91104 are based on a proprietary salt form and formulation of niclosamide, which can be administered locally to the respiratory tract.

The randomised, placebo-controlled, double-blinded, multi-ascending dose trial enrolled 44 healthy subjects. They were grouped into five cohorts, where 34 individuals received UNI911 and ten subjects were given placebo.

 According to the results, the trial met all its endpoints and showed that the concentrated niclosamide solution was well tolerated on administering intranasally and through inhaled route.

In the study, dose-proportional pharmacokinetic was observed with no indications of systemic accumulation of the drug in the blood.

UNION therapeutics chief scientific officer professor Morten Sommer said: “With these promising results for safety and tolerance, the Covid-19 products of UNION therapeutics are gaining substantial interest from platform trials across the world.”

With this encouraging safety and pharmacokinetic results of inhaled and intranasal niclosamide, the company noted that the products will be analysed as a potential treatment (UNI91104) and prophylaxis (UNI91103) for Covid-19.

In a separate development, the National Institutes of Health (NIH) has selected NeuroRx’s Aviptadil as one of two drugs to be analysed in Phase III multi-center clinical trial to be conducted in the US as well as several countries.

Syneos Health and Science 37 partner for decentralised trial delivery

Syneos Health has reached a strategic collaboration with Science 37 to enable the delivery of decentralised clinical trials.

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The integration of Science 37’s technology-first decentralised clinical trial operating system into Syneos Health’s decentralised solutions helps to deliver such clinical trials.

Science 37 and Syneos Health will together provide a unified, seamless technology platform to biopharmaceutical sponsors to streamline their workflow.

 Syneos Health’s decentralised solutions are combined with deep behavioural and therapeutic insights and agile technologies to provide increased clinical trials access to patients and transform product development.

The company stated that Science 37’s premier technology platform comprises data regarding patient communities, telemedicine investigators, mobile nurses, remote coordinators, and connected devices and makes clinical trials virtual.

 

Syneos Health CEO Alistair Macdonald said: “Increasing clinical trial access and diversity is a scientific, business and ethical imperative as we continually look for ways to improve patient outcomes and eliminate healthcare disparities.

“Our powerful partnership with Science 37 adds their industry-leading platform to our Decentralized Solutions and, when combined with the mobile research nursing capabilities delivered through our Illingworth Research team, we’re able to open new pathways toward the long-sought goal of placing patients at the centre of clinical research.”

Science 37 is part of the Syneos Health Dynamic Assembly network, an open ecosystem of data and technology collaborators to deliver solutions designed to address the nuances of each customer engagement.

Pharmaxis to start world-first trial of scar-reducing wound treatment

Australian pharmaceutical research company Pharmaxis has teamed up with the University of Western Australia (UWA) to start a world-first clinical trial to investigate a cream to stop scars forming after trauma, particularly following burn injuries.

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Australian pharmaceutical research company Pharmaxis has teamed up with the University of Western Australia (UWA) to start a world-first clinical trial to investigate a cream to stop scars forming after trauma, particularly following burn injuries.

The trial will be led by prominent surgeon and burns expert Professor Fiona Wood and her team from UWA and researchers from Fiona Stanley Hospital in Murdoch, Western Australia.

Together they will test Pharmaxis’s topical discovery, known as PXS-6302, which has shown promising pre-clinical results in restraining the enzymes that play a significant role in the development of scar tissue.

 “It’s exciting for the research team to explore a novel path to reduce scarring and to be moving closer to that goal,” said Professor Fiona Wood.

“Scar-less healing is the vision that has motivated our work over many decades.”

 “Current treatments aim to rectify the scar in the acute phase such as during wound healing and scar maturation through options such as compression therapy, silicone gel sheeting or when the scar is established by cryotherapy, scar revision or laser, with limited outcomes at times,” said senior research fellow at UWA’s School of Biomedical Sciences Dr Kylie Sandy-Hodgetts.

“This new compound may potentially avoid the need for invasive procedures such as further surgery or laser procedures.”

The pioneering human trial will first evaluate the safety and tolerability of the product in healthy volunteers before conducting further trials in burns and surgical patients.

CDSCO has not recommended for grant of Permission for Emergency use to Pfizer COVID-19 Vaccine

The SEC committee noted that incidents of Palsy, anaphylaxis and other SAEs have been reported during the post marketing and the causality of the events with the vaccines is being investigated. Further Pfizer has not proposed any plan to generate safety and Immunogenicity data in Indian Population.

After the CDSCO decision, Pfizer Inc has withdrawn an application for emergency-use authorization of its COVID-19 vaccine in India that it has developed with Germany’s BioNTech, the company told Reuters on Friday.

The US-based pharma company, which was the first drugmaker to apply for emergency use authorization of its COVID-19 vaccine in the country, had a meeting with India’s drugs regulator on Wednesday and the decision was made after that, the company said.

Pfizer will continue to engage with the authority and resubmit its approval request with additional information as it becomes available in the near future, the statement said.

“Pfizer remains committed to making its vaccine available for use by the Government in India and to pursuing the requisite pathway for emergency use authorisation that enables the availability of this vaccine for any future deployment,” the spokesperson said.

In response, the Indian drug regulator committee said not recommended granting permission for emergency use for Pfizer’s Covid-19 vaccine .

In a statement, the CDSCO’s expert committee said, “Pfizer did not propose any plan to generate safety and immunogenicity data in Indian population.”

The committee also said that it noted side effects reported abroad, causality of events being investigated.

US Pharma giant to set up global R&D headquarters in Ahmedabad

Baxter, a United States-headquartered pharmaceutical giant, will invest around Rs 100 crore to set up its global research and development (R&D) headquarters in Ahmedabad, a senior state government official said.

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“Baxter, one of the largest pharmaceutical companies with a turnover of almost Rs 90,000 crore will be setting up its global R&D headquarters in Ahmedabad. The size of the investment will be around Rs 100 crore. This unit will not only offer specialised roles but also bring a new enthusiasm in the state’s pharmaceutical sector,” M K Das, additional chief secretary to the chief minister, said.

The official said the company has purchased space near Ahmedabad for the project. “On the lines of the Aatmanirbhar Bharat vision, Gujarat extends support to private companies willing to set up R&D units in the state,” Das said.

Currently, Baxter has a research and development and information technology centre in Bengaluru and a manufacturing unit in Ahmedabad where the company is manufacturing generic injectables.

According to industry sources, Baxter has taken up 44,000 square feet (carpet area) in a new commercial office building on Bopal-Ambli BRTS corridor, which has a market value of around Rs 100-110 crore. A questionnaire sent to the company in this regard remained unanswered.

Currently, Gujarat accounts for 33 per cent of India’s pharmaceuticals output. The state exported products worth USD 4 billion in 2019-20, accounting for 28 per cent of India’s pharmaceutical exports. The state also has 40 per cent of India’s contract research organisations, over 130 USFDA approved units, and over 800 WHO GMP compliant units.

CureVac begins Phase III trial of Covid-19 vaccine candidate

Clinical-stage biopharma company CureVac has announced the initiation of Phase III clinical study of its Covid-19 vaccine, CVnCoV, in healthcare workers at the University Medical Center Mainz, Germany.

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Clinical-stage biopharma company CureVac has announced the initiation of Phase III clinical study of its Covid-19 vaccine, CVnCoV, in healthcare workers at the University Medical Center Mainz, Germany.

CVnCoV is an optimised, non-chemically modified mRNA, encoding the prefusion stabilised full-length spike protein of the SARS-CoV-2.

The randomised, observer-blind, placebo-controlled clinical Phase III study aims to analyse the safety and immunogenicity of CVnCoV given as a two-dose schedule of 12µg.

 The study will enrol more than 2,500 participants aged 18 years or above. They will be randomised into this study out of the non-interventional trial.

It complements another global pivotal Phase IIb/III HERALD trial of CVnCoV, which began recently, in more than 35,000 participants.

 CureVac Infectious Diseases head Dr Lidia Oostvogels said: “With this clinical study in healthcare workers, we aim to investigate the difference our vaccine candidate can make in this specific group of individuals who are at particularly high risk of potential infection due to viral exposure.

“Based on this trial, we hope to gain additional insights for effective prevention of Covid-19 in this vulnerable population.”

The latest trial comes after an epidemiological, non-interventional study on healthcare workers from the University Hospital in Mainz.

It enrolled 3,600 hospital employees and also includes medicine and dentistry students.

The ongoing study is analysing the distribution (epidemiology) of Covid-19 in a collective of hospital employees.

It focuses on the rate at which SARS-CoV-2-specific antibodies arise and can be identified in hospital employees as well as the frequency of virologically confirmed Covid-19 cases in them.

Last month, CureVac reported that the ongoing Phase I study of CVnCoV showed that it was well-tolerated across all tested doses ranging from 2µg to 12µg and induced strong binding and neutralising antibody responses.

Boehringer initiates trial of novel SARS-CoV-2 neutralising antibody

Boehringer Ingelheim, Cologne University Hospital (UKK), University of Marburg (UMR) and the German Center for Infection Research (DZIF) have initiated Phase I/IIa clinical investigation of novel SARS-CoV-2 neutralising antibody, BI 767551.

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Boehringer Ingelheim, Cologne University Hospital (UKK), University of Marburg (UMR) and the German Center for Infection Research (DZIF) have initiated Phase I/IIa clinical investigation of novel SARS-CoV-2 neutralising antibody, BI 767551.

A potent anti-SARS-CoV-2 antibody, BI 767551 (DZIF-10c) has demonstrated promising virus neutralising properties in pre-clinical studies.

Merging UKK, UMR and DZIF’s expertise in virology, immunology and clinical investigation with Boehringer Ingelheim’s capabilities in developing and manufacturing therapeutic antibodies, BI 767551 was developed as a potential new therapeutic and preventive/prophylactic option for Covid-19.

 To be led by UKK professors Florian Klein and Gerd Fätkenheuer, the study will be supplied with the antibody by Boehringer Ingelheim.

The Phase I/IIa studies will analyse the safety, pharmacokinetics and antiviral activity of the antibody. The first patients for the study have been enrolled.

 In Phase I part of the study, participants will be given a single infusion or a single inhalation of the antibody.

Late-stage confirmatory studies will be conducted if BI 767551 is observed to be well tolerated.

Boehringer Ingelheim Innovation Unit Board of Managing Directors member Michel Pairet said: “We are excited to contribute to the development of BI 767551 in collaboration with our partners, with the aim to provide an innovative SARS-CoV-2 neutralising antibody, combining a systemic with an inhaled route of administration.”

University of Marburg Institute of Virology Director and DZIF Emerging Infections coordinator Prof Stephan Becker said: “Monoclonal antibodies are a promising component in the fight against new viruses, such as the SARS-CoV-2.

“If this antibody turns out to be effective against COVID-19, this finding could be helpful in the current and also in future epidemics and pandemics.”

Last month, the Icahn School of Medicine at Mount Sinai, Department of Medicine’s Clinical Trials Office and Boehringer Ingelheim enrolled the first patient to evaluate nintedanib in adult patients with acute lung injury following Covid-19 infection.

EMA Server Breached, Hackers Steal Pfizer/BioNTech Vaccine Data

LONDON (Reuters) – U.S. drugmaker Pfizer and its German partner BioNTech said on Wednesday that documents related to development of their COVID-19 vaccine had been “unlawfully accessed” in a cyberattack on Europe’s medicines regulator.

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The European Medicines Agency (EMA), which assesses medicines and vaccines for the European Union, said hours earlier it had been targeted in a cyberattack. It gave no further details.

Pfizer and BioNTech said they did not believe any personal data of trial participants had been compromised and EMA “has assured us that the cyber attack will have no impact on the timeline for its review.”

It was not immediately clear when or how the attack took place, who was responsible or what other information may have been compromised.

The two companies said they had been informed by the EMA “that the agency has been subject to a cyber attack and that some documents relating to the regulatory submission for Pfizer and BioNTech’s COVID-19 vaccine candidate” had been viewed.

Such documents could be extremely valuable to other countries and companies rushing to develop vaccines, experts said.

 

“When it comes to the data submitted to these kinds of regulatory bodies, we are talking confidential information about the vaccine and its mechanism of action, its efficiency, its risks & known possible side effects and any unique aspects such as handling guidelines,” said Marc Rogers, founder of a volunteer group fighting Covid-related breaches, CTI-League.

“It also provides detailed information on other parties involved in the supply and distribution of the vaccine and potentially significantly increases the attack surface for the vaccine,” adding more ways the formulas or production could be hacked or stolen.

The companies said “no BioNTech or Pfizer systems have been breached in connection with this incident and we are unaware that any study participants have been identified through the data being accessed.”

A spokeswoman for BioNTech declined further comment. Pfizer did not respond to a request for further comment.

The Pfizer-BioNTech vaccine is a top contender in the global race to beat back COVID-19. It is already being administered in Britain.

The EMA has said it would complete its review by Dec. 29, although its schedule may change.

The EMA statement gave few details about the attack, saying only it was investigating with help from law enforcement.

“EMA cannot provide additional details whilst the investigation is ongoing,” it said in a statement.

U.S. law enforcement and cybersecurity officials did not respond to requests for comment.

Hacking attempts against healthcare and medical organisations have intensified during the COVID-19 pandemic as attackers ranging from state-backed spies to cyber criminals hunt for information.

 

Reuters has previously reported on allegations that hackers linked to North Korea, South Korea, Iran, Vietnam, China and Russia have on separate occasions tried to steal information about the virus and potential treatments.

Reuters has documented that espionage campaigns targeted a slew of pharmaceutical and vaccine development companies including Gilead, Johnson & Johnson, Novavax, and Moderna. Regulators and international organizations such as the World Health Organization have also come under repeated attack.

“Vaccine candidates represent liquid gold to many parties, both in terms of the opportunity and the pure market value,” said Rogers, who is also vice president at security company Okta Inc. “Information on the vaccine and access to any link in the distribution chain has significantly increased value.”

The respiratory virus, which emerged in China in late 2019, has infected more than 68 million people worldwide, according to a Reuters tally. More than 1.5 million people have died.

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