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Vinflunine

Vinflunine is a science topic covered in the lgStudy science library. This page brings together a partial reference excerpt, illustrations, worked examples, real-world applications and a short study plan, so you can understand Vinflunine rather than just read about it. In short: Vinflunine (INN, trade name Javlor) is a novel fluorinated vinca alkaloid derivative undergoing research for the treatment of bladder cancer. It was originally discovered by the team of the Professor Jean-Claude Jacquesy (UMR CNRS 6514 – Poitiers University), developed by Laboratoires Pierre Fabre and was licensed to Bristol-Myers Squibb for development in certain countries, including the United States.

Vinflunine — main illustration
Vinflunine — illustration

Key takeaways

  • Vinflunine belongs to science; place it in that map before memorising details.
  • Learn the definition first, then one example that makes the definition concrete.
  • Connect Vinflunine to a quantity you can measure, compute or draw — that is where exam questions come from.
  • Reproduce the core statement of Vinflunine from memory before moving on to harder problems.

Reference excerpt

Vinflunine (INN, trade name Javlor) is a novel fluorinated vinca alkaloid derivative undergoing research for the treatment of bladder cancer. It was originally discovered by the team of the Professor Jean-Claude Jacquesy (UMR CNRS 6514 – Poitiers University), developed by Laboratoires Pierre Fabre and was licensed to Bristol-Myers Squibb for development in certain countries, including the United States. On November 23, 2007, Pierre Fabre Medicament and Bristol-Myers Squibb announced that they were terminating their license agreement for the development of vinflunine, and that Pierre Fabre were continuing "discussions with regulatory authorities and plan to file for the registration of vinflunine for bladder cancer in the first quarter of 2008."

Approvals and indications As of 2012, vinflunine was registered for use in Australia for "advanced or metastatic transitional cell carcinoma of the urothelial tract after failure of a prior platinum containing regimen," but is not covered under the Pharmaceutical Benefits Scheme. As of 2016, vinflunine was the only commercially-approved agent in some countries for salvage therapy of urothelial carcinoma, (with approval based on the results of a phase III trial), with a reported median OS of about 6 months.

Clinical trials It has undergone a phase III clinical trial for advanced transitional cell carcinoma of the urothelial tract.

References

External links "Vinflunine". Drug Information Portal. U.S. National Library of Medicine. Archived from the original on February 2, 2021.

Illustrations

Vinflunine illustration

Worked examples

Example 1 — a first encounter with Vinflunine

Start with the simplest possible case. Write down what Vinflunine claims or describes in one sentence, then invent the smallest concrete situation in which that sentence is true. In science, the smallest case is usually a single object, a single equation or a single measurement. Check that every symbol or term in your sentence has a meaning in that case.

Example 2 — changing one variable

Take the situation from Example 1 and change exactly one quantity: double it, halve it, or set it to zero. Predict what should happen to Vinflunine before you calculate. Comparing your prediction with the result is the fastest way to find out whether you understand the idea or only the words.

Example 3 — an exam-style question

Typical questions about Vinflunine ask you to (a) state it precisely, (b) apply it to given data, and (c) explain a limitation. Practise writing all three answers in under five minutes; the third part is what separates a full-mark answer from an average one.

Applications of Vinflunine

In research
Vinflunine appears in science research whenever the underlying quantities have to be modelled precisely. Papers usually cite it as a starting assumption and then explore where it breaks down.
In technology and industry
Engineering practice reuses Vinflunine in design rules, simulations and safety margins. Knowing the idea lets you read a specification sheet and understand why the numbers look the way they do.
In the classroom
Vinflunine is common in secondary-school and first-year university syllabi. It links to neighbouring topics Acetate esters, Drugs developed by Bristol Myers Squibb, Indole alkaloids, so understanding it makes those chapters shorter.
In everyday life
Look for Vinflunine outside the textbook — in sport, cooking, traffic, electronics or the sky above you. An example you found yourself is remembered far longer than one you were given.
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How to study Vinflunine in 20 minutes

  1. Read the reference excerpt below once, without taking notes.
  2. Close the page and write down what Vinflunine means in your own words.
  3. Compare your version with the excerpt and mark what you missed.
  4. Work through the three examples above with pen and paper.
  5. Explain Vinflunine out loud to somebody else — or to Teacher Smith in the lgStudy chat.

Frequently asked questions

What is Vinflunine in simple terms?

Vinflunine (INN, trade name Javlor) is a novel fluorinated vinca alkaloid derivative undergoing research for the treatment of bladder cancer. It was originally discovered by the team of the Professor Jean-Claude Jacquesy (UMR CNRS 6514 – Poitiers University), developed by Laboratoires Pierre Fabre…

Why does Vinflunine matter?

Because it connects several science ideas at once: it gives you a definition you can apply, a quantity you can calculate, and a way to check whether a result is plausible.

How should I study Vinflunine?

Read the excerpt, restate it from memory, then work through the examples and applications listed on this page. The five-step study plan above takes about twenty minutes.

What does this page cover?

It gives you a compact reference excerpt plus original lgStudy explanations, examples, applications and study material on Vinflunine.

Tags

  • Acetate esters
  • Drugs developed by Bristol Myers Squibb
  • Indole alkaloids
  • Methyl esters
  • Mitotic inhibitors
  • Organofluorides
  • Quinoline alkaloids
  • Vinca alkaloids

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