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Expert Insights: Development and Manufacture of Highly Potent Oral Liquids

XTalks

From a market perspective, the oral liquid segment is anticipated to grow at a compound annual growth rate (CAGR) of approximately 6.5% Best practices include the use of contained engineering solutions to safeguard drug product integrity and protect operators. Dosing flexibility is another prominent advantage provided by PDFs.

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PureTech Reveals New CBD Pill to Rival Jazz’s Epidiolex

XTalks

Clinical-stage biotech company PureTech Health has announced it has developed a new oral CBD therapeutic candidate with improved bioavailability and tolerability, which could expand use of the CBD prodrug in a wide range of indications and age groups. Epidiolex contains sesame seed oil, restricting its use for some individuals.

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Compliance to convenience: understanding the latest innovations in capsule formulation

Pharmaceutical Technology

Softgel capsules, containing a liquid, paste or emulsion active ingredient, are trusted and favoured by many patients. They also offer enhanced bioavailability, exact dosing and an extended shelf life. Softgels have now achieved strong recognition in the prescription, consumer health and supplements markets.

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EverGrain’s Line of Barley-Based Products Scores Upcycled Certification

XTalks

In terms of its nutritional profile, EverPro is high in bioavailable protein, low in carbohydrates, contains just half a gram of sugar per 100 grams and is free from cholesterol, dairy and soy. Both Bright Barley and EverGrain are tapping into the massive global barley market, which is estimated to reach $24.7

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Solving pharma’s process development challenges one API at a time

Pharmaceutical Technology

Yet commercialising a drug is no easy journey, hence why just 10% of new drug candidates succeed in making it to market. Milling is a central part of powder processing, as this is where coarse particles are broken down into smaller ones for a variety of processability, bioavailability, reactivity, and safety-related reasons.

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Calliditas Announces Full Enrollment of the Phase 3 NefIgArd Trial

The Pharma Data

Part B is designed to be a confirmatory post-market approval observational trial to confirm long-term renal protection and assess the difference in kidney function between treated and placebo patients as measured by eGFR over a two-year period from the start of dosing of each patient. It also showed that Nefecon was generally well-tolerated.

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ProstaStream

The Pharma Data

The natural green tea contained by this formula, and the broccoli leaf extracts are also powerful ingredients. Frank Neal is a pen name used for marketing purposes and to protect the author’s identity. It’s less than what you’d pay for fancy exotic groceries that you don’t even like eating.