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Home / Therapeutics - Page 36

Therapeutics

Anixa Biosciences Covid-19 therapy demonstrated comparable potency to remdesivir in pre-clinical testing
Biotechnology | COVID-19 | Infectious Disease | Therapeutics | Vaccine

Anixa Biosciences Covid-19 therapy demonstrated comparable potency to remdesivir in pre-clinical testing

On Dec. 14, 2020, Anixa Biosciences announced that it and partner OntoChem GmbH had verified that one of…

Read More Anixa Biosciences Covid-19 therapy demonstrated comparable potency to remdesivir in pre-clinical testingContinue

CIRM-funded project targeting sickle cell disease received green light for clinical trial
Biotechnology | CRISPR | FDA | Therapeutics

CIRM-funded project targeting sickle cell disease received green light for clinical trial

On Dec.14, 2020, the US Food and Drug Administration (FDA) announced they had granted Investigational New Drug (IND)…

Read More CIRM-funded project targeting sickle cell disease received green light for clinical trialContinue

Incyte announced results of phase 3 study of Ruxolitinib (Jakafi) as treatment for patients with COVID-19 associated cytokine storm
Biotechnology | COVID-19 | Therapeutics

Incyte announced results of phase 3 study of Ruxolitinib (Jakafi) as treatment for patients with COVID-19 associated cytokine storm

On Dec. 14, 2020, Incyte announced that the Phase 3 RUXCOVID study evaluating the safety and efficacy of…

Read More Incyte announced results of phase 3 study of Ruxolitinib (Jakafi) as treatment for patients with COVID-19 associated cytokine stormContinue

AI test ruled out a COVID-19 diagnosis within one hour in Emergency Departments
Artificial Intelligence | Biology | COVID-19 | Infectious Disease | Therapeutics

AI test ruled out a COVID-19 diagnosis within one hour in Emergency Departments

On Dev. 11, 2020, the University of Oxford reported that an Artificial Intelligence test had been shown to…

Read More AI test ruled out a COVID-19 diagnosis within one hour in Emergency DepartmentsContinue

Data from ACTT-2 trial of Baricitinib in hospitalized COVID-19 patients supportive of the EUA published in NEJM
COVID-19 | FDA | Therapeutics

Data from ACTT-2 trial of Baricitinib in hospitalized COVID-19 patients supportive of the EUA published in NEJM

On Dec. 11, 2020, Eli Lilly and Incyte announced The New England Journal of Medicine had published the…

Read More Data from ACTT-2 trial of Baricitinib in hospitalized COVID-19 patients supportive of the EUA published in NEJMContinue

Matinas BioPharma announced collaboration with NIAID to evaluate Gilead’s antiviral remdesivir
Biotechnology | COVID-19 | Nanotechnology | Therapeutics

Matinas BioPharma announced collaboration with NIAID to evaluate Gilead’s antiviral remdesivir

On Dec. 7, 2020, Matinas BioPharma announced that they planned to collaborate with the National Institute of Allergy…

Read More Matinas BioPharma announced collaboration with NIAID to evaluate Gilead’s antiviral remdesivirContinue

High-dose influenza vaccine showed no additional benefit for heart disease patients
Biotechnology | Disease | Infectious Disease | Influenza | Therapeutics | Vaccine

High-dose influenza vaccine showed no additional benefit for heart disease patients

On Dec. 4, 2020, it was reported in JAMA that high-dose influenza (commonly known as flu) vaccines are…

Read More High-dose influenza vaccine showed no additional benefit for heart disease patientsContinue

US DoD awarded $25 million contract to Hollingsworth & Vose to increase production capacity of filtration media
COVID-19 | Medical Device | Therapeutics

US DoD awarded $25 million contract to Hollingsworth & Vose to increase production capacity of filtration media

On Dec. 3, 2020, the U.S. Department of Defense in coordination with the Department of HHS, awarded a…

Read More US DoD awarded $25 million contract to Hollingsworth & Vose to increase production capacity of filtration mediaContinue

University of Oregon opened the Phil and Penny Knight Campus for Accelerating Scientific Impact
Biotechnology | Diagnostics | Disease | Medicine | Therapeutics

University of Oregon opened the Phil and Penny Knight Campus for Accelerating Scientific Impact

On Dec. 2, 2020, the University of Oregon opened the Phil and Penny Knight Campus for Accelerating Scientific…

Read More University of Oregon opened the Phil and Penny Knight Campus for Accelerating Scientific ImpactContinue

Mateon announced development update for ARTIVEDA/ARTISHIELD against COVID-19
Biotechnology | COVID-19 | Therapeutics | WHO

Mateon announced development update for ARTIVEDA/ARTISHIELD against COVID-19

On Nov. 30, 2020, Mateon Therapeutics announced that the India arm of ARTI-19 global study was on track…

Read More Mateon announced development update for ARTIVEDA/ARTISHIELD against COVID-19Continue

Innovation Pharma’s COVID-19 clinical trial supported development of Brilacidin as ‘Pan-Coronavirus’ therapeutic
Biotechnology | COVID-19 | Therapeutics

Innovation Pharma’s COVID-19 clinical trial supported development of Brilacidin as ‘Pan-Coronavirus’ therapeutic

On Nov. 30, 2020, Innovation Pharmaceuticals announced additional independent preliminary laboratory research suggests Brilacidin, the Company’s flagship defensin…

Read More Innovation Pharma’s COVID-19 clinical trial supported development of Brilacidin as ‘Pan-Coronavirus’ therapeuticContinue

RedHill Biopharma expanded U.S.-based manufacturing capacity of opaganib for COVID-19
Biotechnology | COVID-19 | Therapeutics

RedHill Biopharma expanded U.S.-based manufacturing capacity of opaganib for COVID-19

On Nov. 25, 2020, RedHill Biopharma announced partnerships with two leading, U.S.-based manufacturers for large-scale manufacturing of opaganib….

Read More RedHill Biopharma expanded U.S.-based manufacturing capacity of opaganib for COVID-19Continue

BioNTech and InstaDeep announce AI Innovation Lab to develop novel immunotherapies
Artificial Intelligence | Biotechnology | Infectious Disease | Therapeutics

BioNTech and InstaDeep announce AI Innovation Lab to develop novel immunotherapies

On Nov. 25, 2020, BioNTech and InstaDeep announced a multi-year strategic collaboration aimed at applying the latest advances…

Read More BioNTech and InstaDeep announce AI Innovation Lab to develop novel immunotherapiesContinue

NeuroRx and Relief announced successful results from expanded use of RLF-100 in patients with COVID-19
Biotechnology | COVID-19 | Disease | Therapeutics | Vaccine

NeuroRx and Relief announced successful results from expanded use of RLF-100 in patients with COVID-19

On Nov. 24, 2020, RELIEF THERAPEUTICS announced that more than 175 patients with Critical COVID-19 and Respiratory Failure…

Read More NeuroRx and Relief announced successful results from expanded use of RLF-100 in patients with COVID-19Continue

AI detected COVID-19 on chest X-rays faster and with more accuracy than radiologists
Biotechnology | COVID-19 | Infectious Disease | Oncology | Radiology | Therapeutics

AI detected COVID-19 on chest X-rays faster and with more accuracy than radiologists

On Nov. 24, 2020, Northwestern University researchers announced they had developed a new artificial intelligence (A.I.) platform that…

Read More AI detected COVID-19 on chest X-rays faster and with more accuracy than radiologistsContinue

Mayo Clinic research confirmed critical role of masks in preventing COVID-19 infection
COVID-19 | Infectious Disease | Non-Profit Research | Therapeutics

Mayo Clinic research confirmed critical role of masks in preventing COVID-19 infection

On Nov. 24, 2020, published data from researchers at Mayo Clinic found that physical separation reduced the exposure…

Read More Mayo Clinic research confirmed critical role of masks in preventing COVID-19 infectionContinue

FDA expanded approval of influenza treatment to post-exposure prevention
Biotechnology | FDA | Infectious Disease | Influenza | Therapeutics

FDA expanded approval of influenza treatment to post-exposure prevention

On Nov. 23, 2020, the U.S. Food and Drug Administration (FDA) expanded the approved indication for Genentech’s Xofluza…

Read More FDA expanded approval of influenza treatment to post-exposure preventionContinue

CytoDyn reached enrollment target of 293 patients for 2nd DSMC interim analysis of phase 3 COVID-19 trial
Biotechnology | COVID-19 | Infectious Disease | Therapeutics

CytoDyn reached enrollment target of 293 patients for 2nd DSMC interim analysis of phase 3 COVID-19 trial

On Nov. 23, 2020, CytoDyn announced it had reached enrollment of 293 patients in its Phase 3 trial…

Read More CytoDyn reached enrollment target of 293 patients for 2nd DSMC interim analysis of phase 3 COVID-19 trialContinue

Study of ‘exceptional responders’ yields clues to cancer and potential treatments
Biotechnology | NIH | Therapeutics

Study of ‘exceptional responders’ yields clues to cancer and potential treatments

On Nov. 19, 2020, in a comprehensive analysis of patients with cancer who had exceptional responses to therapy,…

Read More Study of ‘exceptional responders’ yields clues to cancer and potential treatmentsContinue

Novartis secured exclusive rights for potential acute respiratory distress syndrome cell therapy
Biotechnology | COVID-19 | Therapeutics

Novartis secured exclusive rights for potential acute respiratory distress syndrome cell therapy

On Nov. 19, 2020, Novartis announced that it had entered into an exclusive worldwide license and collaboration agreement…

Read More Novartis secured exclusive rights for potential acute respiratory distress syndrome cell therapyContinue

Medigen Vaccines announced publication of positive results from preclinical studies of COVID-19 vaccine candidate
Biotechnology | COVID-19 | Therapeutics | Vaccine

Medigen Vaccines announced publication of positive results from preclinical studies of COVID-19 vaccine candidate

On Nov. 19, 2020, Medigen Vaccine Biologics announced that preclinical results of their COVID-19 vaccine candidate had been…

Read More Medigen Vaccines announced publication of positive results from preclinical studies of COVID-19 vaccine candidateContinue

Baricitinib received Emergency Use Authorization from FDA for treatment of hospitalized patients with COVID-19
Biotechnology | COVID-19 | FDA | Therapeutics

Baricitinib received Emergency Use Authorization from FDA for treatment of hospitalized patients with COVID-19

On Nov. 19, 2020, Eli Lilly and Incyte announced that the FDA had issued an Emergency Use Authorization…

Read More Baricitinib received Emergency Use Authorization from FDA for treatment of hospitalized patients with COVID-19Continue

XBiotech data showed effective anti-virus activity for antibodies in candidate influenza-COVID-19 therapeutic
Biotechnology | COVID-19 | Diagnostics | Infectious Disease | Influenza | Therapeutics

XBiotech data showed effective anti-virus activity for antibodies in candidate influenza-COVID-19 therapeutic

On Nov. 19, 2020, XBiotech announced data for its breakthrough candidate therapy for treating infections of influenza and…

Read More XBiotech data showed effective anti-virus activity for antibodies in candidate influenza-COVID-19 therapeuticContinue

Gilead announced long-acting HIV-1 capsid inhibitor, lenacapavir, achieved primary endpoint in phase 2/3 study
Biotechnology | HIV | Therapeutics

Gilead announced long-acting HIV-1 capsid inhibitor, lenacapavir, achieved primary endpoint in phase 2/3 study

On Nov. 18, 2020, Gilead Sciences announced topline results from the Phase 2/3 CAPELLA trial evaluating the company’s…

Read More Gilead announced long-acting HIV-1 capsid inhibitor, lenacapavir, achieved primary endpoint in phase 2/3 studyContinue

RedHill’s second COVID-19 candidate cleared by FDA for phase 2/3 Study in symptomatic COVID-19 disease
Biotechnology | COVID-19 | FDA | Therapeutics

RedHill’s second COVID-19 candidate cleared by FDA for phase 2/3 Study in symptomatic COVID-19 disease

On Nov. 17, 2020, RedHill Biopharma announced that the U.S. Food and Drug Administration (FDA) had cleared the…

Read More RedHill’s second COVID-19 candidate cleared by FDA for phase 2/3 Study in symptomatic COVID-19 diseaseContinue

Mayo Clinic reported 900 employees contracted COVID-19 from local community
Biotechnology | COVID-19 | Therapeutics

Mayo Clinic reported 900 employees contracted COVID-19 from local community

On Nov. 17, 2020, the Mayo Clinic reported that more than 900 employees had contracted COVID-19 in the…

Read More Mayo Clinic reported 900 employees contracted COVID-19 from local communityContinue

RedHill completed enrollment for COVID-19 US phase 2 study with opaganib
Biotechnology | COVID-19 | Therapeutics

RedHill completed enrollment for COVID-19 US phase 2 study with opaganib

On Nov. 16, 2020, RedHill Biopharma announced that the U.S. Phase 2 study with opaganib (Yeliva, ABC294640)1 in…

Read More RedHill completed enrollment for COVID-19 US phase 2 study with opaganibContinue

Wellcome Sanger Institute and COG-UK received £122M UK investment for COVID-19 genomic surveillance
Biotechnology | COVID-19 | Diagnostics | Genomics | Infectious Disease | Therapeutics | Vaccine

Wellcome Sanger Institute and COG-UK received £122M UK investment for COVID-19 genomic surveillance

On Nov. 16, 2020, the UK Department for Health and Social Care Testing Innovation Fund announced £12.2M funding…

Read More Wellcome Sanger Institute and COG-UK received £122M UK investment for COVID-19 genomic surveillanceContinue

Swissmedic began rolling review of Moderna’s mRNA vaccine against COVID-19
Biotechnology | COVID-19 | Infectious Disease | Therapeutics | Vaccine

Swissmedic began rolling review of Moderna’s mRNA vaccine against COVID-19

On Nov. 13, 2020, Moderna announced that Swissmedic had started a rolling review of mRNA-1273, the Company’s vaccine…

Read More Swissmedic began rolling review of Moderna’s mRNA vaccine against COVID-19Continue

CHMP recommended EU approval of Roche’s Xofluza (baloxavir marboxil) for the treatment of influenza
Biotechnology | Infectious Disease | Influenza | Therapeutics

CHMP recommended EU approval of Roche’s Xofluza (baloxavir marboxil) for the treatment of influenza

On Nov. 13, 2020, Roche announced that the European Medicines Agency’s (EMA) Committee for Medicinal Products for Human…

Read More CHMP recommended EU approval of Roche’s Xofluza (baloxavir marboxil) for the treatment of influenzaContinue

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