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Related Concept Videos

Drug toxicity: Drug–Drug Interaction01:30

Drug toxicity: Drug–Drug Interaction

22
Drug–drug interactions can precipitate toxicity through multiple mechanisms. Absorption interactions alter how drugs enter the body, exemplified when ranitidine increases the absorption of basic drugs, while cholestyramine decreases the levels of propranolol. Protein binding interactions occur when drugs share the same binding sites on plasma proteins. Drugs like aspirin and warfarin, when bound in excess, can lead to increased free drug concentrations, enhancing the potential for...
22
FDA Approved Drugs: Changes to Approved Drugs01:26

FDA Approved Drugs: Changes to Approved Drugs

279
Post-approval, manufacturers may modify an approved new or generic drug product. Such modifications can encompass alterations in the Active Pharmaceutical Ingredient (API), manufacturing process, formulation, batch size, manufacturing site, and container closure system (FDA Guidance for Industry, April 2004). Often, a drug product may undergo multiple changes.These modifications require careful evaluation to determine their potential impact on the drug product's identity, strength, quality,...
279
Bioequivalence of Drugs: Drugs with Multiple Indications01:09

Bioequivalence of Drugs: Drugs with Multiple Indications

167
The concept of therapeutic equivalence (TE) in drugs with multiple indications is complex. A generic drug may be therapeutically equivalent to a brand-name product for one specific indication, but this doesn't necessarily mean it's equivalent for all other indications. Evidence of TE in one patient group and bioequivalence shown in healthy volunteers can support—but not confirm—TE for other indications. However, definitive proof requires individual clinical studies for each...
167
Pharmacokinetics: Drug–Drug Interactions01:25

Pharmacokinetics: Drug–Drug Interactions

477
Drug interactions occur when the pharmacological effect of one drug is altered by another substance, either enhancing or diminishing its activity. The drug whose activity is altered is known as the object drug, and the substance causing the alteration is called the agent drug or the precipitant. The net effects of these interactions are mostly undesirable, leading to decreased effectiveness or increased adverse effects. In rare cases, interactions can be beneficial, such as the enhanced...
477
Tissue-Drug Binding: Localization of Drugs and its Significance01:24

Tissue-Drug Binding: Localization of Drugs and its Significance

475
Body tissues, comprising approximately 40% of the body weight, are crucial in drug distribution and localization. These tissues can serve as drug storage sites, competing with plasma binding sites for drug molecules.
Drugs can bind to different tissue components, enhancing their distribution and localization. The factors influencing drug localization in tissues include the drug's lipophilicity, structural characteristics, tissue perfusion rate, and pH differences. These factors determine...
475
Factors Affecting Protein-Drug Binding: Drug Interactions01:23

Factors Affecting Protein-Drug Binding: Drug Interactions

633
Drug interactions are a critical aspect of pharmacology and can occur when two or more drugs compete for the same binding site. This competition can result in one drug displacing another, altering the effect of the displaced drug. Drug interactions are complex processes that rely heavily on how much of the displacer drug is present and how strongly it can bind to the same sites as the displaced drug.
Displacement interactions can have varying outcomes, ranging from toxicity to virtually...
633

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A Computerized Test Battery to Study Pharmacodynamic Effects on the Central Nervous System of Cholinergic Drugs in Early Phase Drug Development
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[New antimalarial drugs]

P Ambroise-Thomas1

  • 1Département de parasitologie-mycologie médicale et moléculaire, UPRES A CNRS 5082 Faculté de médecine Université Joseph-Fourier, Grenoble, La Tronche.

La Revue Du Praticien
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Summary
This summary is machine-generated.

Drug resistance in Plasmodia necessitates new antimalarial development. Current drug discovery and evaluation face challenges in meeting international standards for efficacy and safety.

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Area of Science:

  • Malariology
  • Pharmacology
  • Infectious Diseases

Background:

  • Increasing Plasmodia resistance to existing antimalarials poses a significant global health challenge.
  • The pipeline for novel antimalarial drugs has been limited, with few new agents introduced recently.
  • Existing drug discovery efforts often lack targeted pharmacological research.

Purpose of the Study:

  • To highlight the urgent need for new antimalarial drug discovery.
  • To assess the current landscape of antimalarial drug development.
  • To identify deficiencies in the clinical and biological evaluation of new antimalarial candidates.

Main Methods:

  • Review of recent antimalarial drug introductions and ongoing investigations.
  • Analysis of drug discovery approaches, distinguishing targeted research from others.
  • Evaluation of current practices in clinical and biological assessment of antimalarials.

Main Results:

  • Only two new antimalarials have emerged recently: artemether IM (Paluther) for severe malaria and a chloroquine-proguanil combination (Savarine) for prophylaxis.
  • A limited number of new antimalarial molecules in development originate from targeted pharmacological research.
  • Clinical and biological evaluations frequently deviate from international industrial guidelines.

Conclusions:

  • There is a critical need for accelerated and improved antimalarial drug discovery.
  • Current evaluation methodologies for new antimalarials may compromise their potential for regulatory approval in Western countries.
  • Ensuring adherence to international standards is crucial for the successful registration and deployment of new antimalarial therapies.