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FDA Approved Drugs: Changes to Approved Drugs01:26

FDA Approved Drugs: Changes to Approved Drugs

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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,...
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Treatment for Pulmonary Arterial Hypertension: Prostacyclin Receptor Agonists01:23

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Prostacyclin receptor agonists are a class of therapeutic agents integral to managing pulmonary arterial hypertension (PAH). These drugs operate by mimicking the action of prostaglandin I2, or PGI2, a naturally occurring compound in the body.
These agonists bind to the IPR receptor situated on the plasma membrane of the pulmonary artery smooth muscle cells. This binding triggers a cascade of reactions known as the GS-AC-cAMP-PKA pathway. This pathway results in the relaxation of smooth muscle...
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Dipeptidyl Peptidase 4 Inhibitors01:23

Dipeptidyl Peptidase 4 Inhibitors

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Dipeptidyl peptidase 4 (DPP-4) is a serine protease widely distributed in the body. It's involved in the inactivation of GLP-1 and GIP hormones, which are crucial for insulin regulation. DPP-4 inhibitors, such as sitagliptin (Januvia), saxagliptin (Onglyza), linagliptin (Tradjenta), alogliptin (Nesina), and vildagliptin (Galvus), help increase the proportion of active GLP-1, enhancing insulin secretion. These inhibitors work by competitively binding to DPP-4. This binding causes a...
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Drug Administration and Therapy Phases: Overview01:26

Drug Administration and Therapy Phases: Overview

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Drugs, the chemical agents used in diagnosing, treating, or preventing diseases, undergo a four-phase process of development: pharmaceutic, pharmacokinetics, pharmacodynamics, and therapeutic.
The pharmaceutical phase focuses on leveraging the physicochemical properties of the drug to design and manufacture an effective product. Variants include orally administered tablets or capsules, topical creams or ointments, and parenteral-delivery solutions or emulsions.
The pharmacokinetic phase...
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Insulin: Dosing Regimen and Adverse Effects01:16

Insulin: Dosing Regimen and Adverse Effects

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Insulin-replacement therapy usually includes both long-acting insulin (basal) and short-acting insulin (to cater to postprandial needs). In a diverse group of type 1 diabetes patients, the average daily insulin dose is typically 0.5-0.7 units/kg body weight. However, obese patients and pubertal adolescents may need more due to insulin resistance.
The basal dose constitutes about 40%-50% of the total daily dose, with the rest as premeal insulin. The mealtime insulin dose should mirror...
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PI3K/mTOR/AKT Signaling Pathway01:22

PI3K/mTOR/AKT Signaling Pathway

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The mammalian target of rapamycin  (mTOR) is a serine/threonine kinase that regulates growth, proliferation, and cell survival in response to hormones, growth factors, or nutrient availability. This kinase exists in two structurally and functionally distinct forms: mTOR complex 1  (mTORC1) and mTOR complex 2  (mTORC2). The first form (mTORC1) is composed of a rapamycin-sensitive Raptor and proline-rich Akt substrate, PRAS40. In contrast,  mTORC2 consists of a...
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Related Experiment Video

Updated: Jan 16, 2026

Scaled-Up Preparation of an Intermediate of Upatinib, ACT051-3
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Ifupinostat: First Approval.

Simon Fung1

  • 1Springer Nature, Private Bag 65901, Mairangi Bay, Auckland, 0754, New Zealand. dru@adis.com.

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|October 1, 2025
PubMed
Summary
This summary is machine-generated.

Ifupinostat, a novel dual phosphoinositide 3-kinase α (PI3Kα)/histone deacetylase (HDAC) inhibitor, has gained its first approval in China. This marks a significant advancement in treating relapsed or refractory diffuse large B-cell lymphoma.

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Area of Science:

  • Oncology
  • Pharmacology
  • Drug Development

Background:

  • Diffuse large B-cell lymphoma (DLBCL) is a significant hematologic malignancy.
  • Relapsed or refractory DLBCL presents a critical unmet medical need.
  • Targeted therapies offer new avenues for managing difficult-to-treat lymphomas.

Purpose of the Study:

  • To summarize the development milestones of ifupinostat.
  • To highlight the first approval of ifupinostat as a monotherapy.
  • To detail its application in relapsed or refractory diffuse large B-cell lymphoma.

Main Methods:

  • Review of preclinical and clinical development data.
  • Analysis of regulatory submission and approval process.
  • Summary of ifupinostat's mechanism of action as a dual PI3Kα/HDAC inhibitor.

Main Results:

  • Ifupinostat received its first approval in China on June 30, 2025.
  • The approval is for adult patients with relapsed or refractory DLBCL after at least two systemic therapies.
  • Continued approval hinges on a confirmatory Phase 3 trial.

Conclusions:

  • Ifupinostat represents a first-in-class dual PI3Kα/HDAC inhibitor.
  • This approval signifies a breakthrough for patients with relapsed/refractory DLBCL.
  • Further clinical evaluation will confirm its long-term efficacy and safety.