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October 05, 2017

Today's Rundown

  1. Thiel, Parker said to fund secretive T-cell biotech startup

  2. Bluebird’s gene therapy halts progression of ‘devastating’ disease cALD

  3. Visterra adds $24M to series C to take flu drug to phase 2b

  4. [Sponsored] End-to-End Drug & Diagnostic Development Support For A New Immuno Oncology Agent

  5. AMR Centre picks up Medivir’s superbug-busting candidate

  6. DDF 2017: Choosing a CRO, and the implications of new R2 regulations

  7. Gold nanoparticles effectively deliver CRISPR to mouse models of DMD

  8. Scientists reverse heart failure via newly discovered regeneration pathway

  9. Most new cancer meds haven't proved they can improve or extend lives: study

Featured Story

Thiel, Parker said to fund secretive T-cell biotech startup

A report from CNBC says that PayPal founder Peter Thiel and Facebook investor Sean Parker are investing in a new, secretive oncology biotech company.

Top Stories

Bluebird’s gene therapy halts progression of ‘devastating’ disease cALD

A single dose of Bluebird Bio’s gene therapy for cerebral adrenoleukodystrophy (cALD) stabilized the disease in 15 of 17 patients over more than two years of follow-up.

Visterra adds $24M to series C to take flu drug to phase 2b

Visterra has extended its series C round to fund the advance of its lead candidate into phase 2b. The extension puts Visterra back on the multifront path through the clinic it plotted out before its aborted IPO attempt.

[Sponsored] End-to-End Drug & Diagnostic Development Support For A New Immuno Oncology Agent

Learn how one company sought support at multiple junctures—from manufacturing to biomarker evaluation to market access—to enable a faster and more effective launch of their new programmed death receptor-1 (PD-1)-blocking antibody.

AMR Centre picks up Medivir’s superbug-busting candidate

AMR Centre has licensed a program from Medivir. The metallo-beta-lactamase inhibitors are designed to inactivate the NDM-1 mechanism, rendering drug-resistant bacteria vulnerable to beta-lactam antibiotics.

DDF 2017: Choosing a CRO, and the implications of new R2 regulations

As part of our video series for this year’s DDF 2017 event, life science leaders spoke to us about CRO needs and new regulations.

Gold nanoparticles effectively deliver CRISPR to mouse models of DMD

CRISPR-Cas9 is a promising tool against genetic disease, but it comes with some safety concerns, namely, off-target gene editing that may bring about harmful side effects such as cancer. UC Berkeley scientists are using a new delivery system to more safely correct the mutated dystrophin gene in mouse models of Duchenne muscular dystrophy.

Scientists reverse heart failure via newly discovered regeneration pathway

A signaling pathway in the body called Hippo is well known in scientific circles for its potential role in cancer, but now scientists at Baylor believe they have found another place where manipulating this system could be beneficial—the heart. When they turned off the pathway in mouse models of heart failure, they were able to restore pumping ability to that of healthy hearts.

Most new cancer meds haven't proved they can improve or extend lives: study

Sixty-eight cancer drug indications won European approval between 2009 and 2013—but most of them did so without showing they could extend or improve life, a new study shows.

Enrollment Showcase

Online Graduate Programs Designed for Your Career

Drexel University’s online graduate programs in biomedicine, clinical research, drug discovery, and molecular medicine were developed with working professionals in mind, providing you with the education, practical skills, and competitive edge you need to be successful in your career. Learn more.

Resources

[Webinar] Validating a 7 Day Membrane Filtration Sterility Test using Celsis®

Join us as we discuss how Charles River Celsis® helped Labor L+S AG validate a 7-day membrane filtration sterility test using existing protocols.

[Whitepaper] Industry Report: Clinical Operations Leaders Reveal Need for Change

The 2017 Unified Clinical Operations Survey finds that 99% of respondents report the need to unify their clinical applications, including CTMS, EDC, eTMF, and study start-up.

[Infographic] Evolution of Flexible Commercial Biologics Manufacturing

Learn how Catalent Biologics is paving the way for flexible biologics development and manufacturing through advanced technologies and fully integrated multi-product facility.

[eBook] Developing Site-specifically Modified ADCs: Using a Chemoenzymatic Approach

Download the eBook to get articles from various Elsevier journals highlighting developments in ADC technology.

[Article] Optimizing titer and use of a specific enzyme for generating a fully processed antibody

Learn how cell development and process scale-up can be optimized for antibodies requiring additional processing.

[Webinar] Within-Subject Clinical Trials: Intro to New Methods & Stat. Models

In this webinar, we will introduce the rapidly-evolving within-subject clinical trial (WSCT) methods for early phase evidence generation that require fewer people, less time, and usually less funding than traditional early phase methods.

Events

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