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What Tech Trends Do Life Sciences Marketers Need to Know About?

PM360

Another capability made possible by fine-tuning is the enhancement of content tagging. Content tagging has always been a labor-intensive task. Auto-tagging ensures that the right content efficiently reaches the right customers. Fine-tuning models can target domains and generate prompts to tag the content into relevant topics.

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The FDA and Aduhelm: WTF?

World of DTC Marketing

Not to mention the $56,000 annual price tag. We think the decision is on very solid ground, that we are on very solid ground when it comes to the data and the rationale for utilizing accelerated approval to greenlight this drug.”. Aduhelm joins a group of drugs that potentially leave patients worse off and much poorer for it.

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You can’t afford to get cancer

World of DTC Marketing

As cancer survival rates rise, so do the price tags of life-saving treatments. Few cancer drugs approved via the accelerated FDA approval pathway were judged to have verified benefits based on improvement in survival reported in confirmatory trials. billion included out-of-pocket costs of $16.22 ScienceNews.com.

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Rare Disease Spotlight – tracing the rise of orphan drug designations over almost 40 years

Pharmaceutical Technology

The US Food and Drug Administration (FDA) put a high-profile bluebird bio trial for sickle cell disease on partial clinical hold, and advisory panels deliberated over decisions involving gene therapies for amyotrophic lateral sclerosis (ALS), cerebral adrenoleukodystrophy (CALD), and beta-thalassemia.

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J&J builds case for antidepressant Spravato with head-to-head trial

pharmaphorum

Johnson & Johnson’s Spravato therapy for treatment-resistant depression (TRD) hasn’t made the impact the company hoped for in the market, and it is looking to new clinical results to accelerate its take-up. The post J&J builds case for antidepressant Spravato with head-to-head trial appeared first on.

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Pioneering the Path Pre- and Post-Launch Strategies

PM360

Areas including trial enrollment or Managed Access Programs, coordination with Patient Advocacy Groups to imbibe patient input into treatment development, product access post-launch, and RWE support for added indications will become the mainstay for Medical Affairs as we move ahead.

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CCC Adds Clinical Trial Registries to RightFind Navigate Data Sources

Copyright Clearance Center

. – CCC , a pioneer in voluntary collective licensing, advancing copyright, accelerating knowledge, and powering innovation, announces Clinical Trial Registries, a new data connector for customers of the cloud-based software solution RightFind Navigate. clinical trials through the connector to ClinicalTrials.gov.