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Home / Therapeutics - Page 31

Therapeutics

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

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

FDA approved Merck’s KEYTRUDA (pembrolizumab) in combination with chemo for patients with TNBC
Biotechnology | Chemical | FDA | Therapeutics

FDA approved Merck’s KEYTRUDA (pembrolizumab) in combination with chemo for patients with TNBC

On Nov. 13, 2020, Merck announced that the U.S. Food and Drug Administration (FDA) had approved KEYTRUDA, Merck’s…

Read More FDA approved Merck’s KEYTRUDA (pembrolizumab) in combination with chemo for patients with TNBCContinue

NeuroRx and Relief Therapeutics announce enrollment of 150 patients in phase 2b/3 trial of RLF-100™ for Critical COVID-19 with Respiratory Failure
Biotechnology | COVID-19 | FDA | Therapeutics

NeuroRx and Relief Therapeutics announce enrollment of 150 patients in phase 2b/3 trial of RLF-100™ for Critical COVID-19 with Respiratory Failure

On Nov. 13, 2020, NeuroRx and Relief Therapeutics announced that to-date, 150 patients (out of a targeted enrollment…

Read More NeuroRx and Relief Therapeutics announce enrollment of 150 patients in phase 2b/3 trial of RLF-100™ for Critical COVID-19 with Respiratory FailureContinue

Agilent received expanded FDA approval for PD-L1 IHC 22C3 pharmDx in triple-negative breast cancer
Biotechnology | FDA | Oncology | Therapeutics

Agilent received expanded FDA approval for PD-L1 IHC 22C3 pharmDx in triple-negative breast cancer

On Nov. 13, 2020, Agilent Technologies announced it had received U.S. Food and Drug Administration (FDA) approval for…

Read More Agilent received expanded FDA approval for PD-L1 IHC 22C3 pharmDx in triple-negative breast cancerContinue

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

CALAVI did not meet the primary endpoint in patients hospitalised with respiratory symptoms of COVID-19
Biotechnology | COVID-19 | Diagnostics | Infectious Disease | Therapeutics

CALAVI did not meet the primary endpoint in patients hospitalised with respiratory symptoms of COVID-19

On Nov. 12, 2020, AstraZeneca announced that the CALAVI Phase II trials for Calquence (acalabrutinib) in patients hospitalised…

Read More CALAVI did not meet the primary endpoint in patients hospitalised with respiratory symptoms of COVID-19Continue

Sorrento announced IND filing for COVI-DROPS against SARS-CoV-2
Biotechnology | COVID-19 | Therapeutics | Vaccine

Sorrento announced IND filing for COVI-DROPS against SARS-CoV-2

On Nov. 11, 2020, Sorrento Therapeutics announced that it was filing an investigational new drug application (IND) for…

Read More Sorrento announced IND filing for COVI-DROPS against SARS-CoV-2Continue

DSMB analysis recommended continuance of P3 COVID-19 ARDS trial
Biotechnology | COVID-19 | Therapeutics

DSMB analysis recommended continuance of P3 COVID-19 ARDS trial

On Nov. 11, 2020, Mesoblast announced that the randomized controlled Phase 3 trial of remestemcel-L in patients with…

Read More DSMB analysis recommended continuance of P3 COVID-19 ARDS trialContinue

Mateon and Windlas Biotech announced agreement to commercialize ARTIVEDA against COVID-19
Biotechnology | COVID-19 | Therapeutics

Mateon and Windlas Biotech announced agreement to commercialize ARTIVEDA against COVID-19

On Nov. 11, 2020, Mateon Therapeutics announced an agreement with Windlas Biotech of India to commercialize ARTIVeda. ARTIVeda…

Read More Mateon and Windlas Biotech announced agreement to commercialize ARTIVEDA against COVID-19Continue

Medigen Vaccines and BlueWillow Biologics partnered to Develop intranasal vaccine for SARS-COV-2
Biotechnology | COVID-19 | Therapeutics | Vaccine

Medigen Vaccines and BlueWillow Biologics partnered to Develop intranasal vaccine for SARS-COV-2

On Nov. 19, 2020, Medigen Vaccine Biologics and BlueWillow Biologics announced a partnership to develop S-2P-NE-01, a nasal…

Read More Medigen Vaccines and BlueWillow Biologics partnered to Develop intranasal vaccine for SARS-COV-2Continue

Long-acting injectable drug prevented HIV in cisgender women
Biotechnology | HIV | NIH | Therapeutics

Long-acting injectable drug prevented HIV in cisgender women

On Nov. 9, 2020, the NIH reported that a pre-exposure prophylaxis (PrEP) regimen containing an investigational long-acting form…

Read More Long-acting injectable drug prevented HIV in cisgender womenContinue

Hydroxychloroquine does not benefit adults hospitalized with COVID-19
Biotechnology | COVID-19 | Infectious Disease | NIH | Therapeutics

Hydroxychloroquine does not benefit adults hospitalized with COVID-19

On Nov. 9, 2020, a National Institutes of Health (NIH) clinical trial evaluating the safety and effectiveness of…

Read More Hydroxychloroquine does not benefit adults hospitalized with COVID-19Continue

Effect of hydroxychloroquine on clinical status at 14 days in hospitalized patients with COVID-19
Biotechnology | COVID-19 | Therapeutics

Effect of hydroxychloroquine on clinical status at 14 days in hospitalized patients with COVID-19

On Nov. 9, 2020, a study published in JAMA reported the effect of hydroxychloroquine on clinical status at…

Read More Effect of hydroxychloroquine on clinical status at 14 days in hospitalized patients with COVID-19Continue

Ultragenyx announced plans to build large-scale gene therapy manufacturing facility for rare diseases
Biotechnology | Disease | Therapeutics

Ultragenyx announced plans to build large-scale gene therapy manufacturing facility for rare diseases

On Nov. 9, 2020, Ultragenyx announced that it planned to build a new large-scale gene therapy manufacturing facility…

Read More Ultragenyx announced plans to build large-scale gene therapy manufacturing facility for rare diseasesContinue

Pfizer and BioNTech announced vaccine candidate against COVID-19 achieved success in interim analysis from phase 3 study
Biotechnology | COVID-19 | Therapeutics | Vaccine

Pfizer and BioNTech announced vaccine candidate against COVID-19 achieved success in interim analysis from phase 3 study

On Nov. 9, 2020, Pfizer and BioNTech announced their mRNA-based vaccine candidate, BNT162b2, against SARS-CoV-2 had demonstrated evidence…

Read More Pfizer and BioNTech announced vaccine candidate against COVID-19 achieved success in interim analysis from phase 3 studyContinue

Humanigen announced CRADA agreement with U.S. government to develop lenzilumab for COVID-19
Biotechnology | COVID-19 | Infectious Disease | Therapeutics

Humanigen announced CRADA agreement with U.S. government to develop lenzilumab for COVID-19

On Nov. 6, 2020, Humanigen announced that it had entered into a Cooperative Research and Development Agreement (CRADA)…

Read More Humanigen announced CRADA agreement with U.S. government to develop lenzilumab for COVID-19Continue

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