This “FTase (Farnesyltransferase) inhibitor - Pipeline Insight, 2024” report provides comprehensive insights about 2+ companies and 2+ pipeline drugs in FTase inhibitor pipeline landscape. It covers the pipeline drug profiles, including clinical and nonclinical stage products. It also covers the therapeutics assessment by product type, stage, route of administration, and molecule type. It further highlights the inactive pipeline products in this space.
FTase catalyzes the post-translational addition of a hydrophobic isoprenoid farnesyl moiety from farnesyl diphosphate (FPP), to a cysteine residue of a protein substrate containing a typical CAAX motif at the carboxyl terminus.
FTase Inhibitors- Farnesyltransferase inhibitors hold considerable promise as anticancer drugs in the clinical studies. Several studies evaluated including the identification of natural products such as the chaetomellic and zaragozic acids that mimic farnesylpyrophosphate, bisubstrate transition state analogs combining elements of the farnesyl and tetrapeptide substrates and peptidomimetics that reproduce features of the carboxyl terminal tetrapeptide CA1A2X sequence. Several farnesyl transferase inhibitors are in clinical development for the treatment of solid tumors.
Lonafarnib: Eiger Bio Pharmaceuticals Lonafarnib (also known as SCH66336) is a tricyclic nonpeptidic farnesyl transferase inhibitor that competes with protein substrates for binding to farnesyl transferase. It blocks the post-translational farnesylation of prelamin A and other proteins that are targets for farnesylation. Farnesylation is essential for the function of both mutant and non-mutant lamin-A proteins, including progerin. Merck originally developed Lonafarnib and subsequently licensed it to EigerBiopharmaceuticals.
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Geography Covered
- Global coverage
FTASE inhibitor Understanding
FTase inhibitor: Overview
Farnesyltransferase (FTase) is a heterodimeric zinc enzyme that belongs to the transferases family. It catalyzes the synthesis of geranylgeranyl diphosphate from Trans, trans-farnesyl diphosphate and isopentenyl diphosphate. Protein farnesyltransferase (FTase) is a two-subunit enzyme that is comprised by a 48 kDa a-subunit and a 46 kDa ß-subunit.FTase catalyzes the post-translational addition of a hydrophobic isoprenoid farnesyl moiety from farnesyl diphosphate (FPP), to a cysteine residue of a protein substrate containing a typical CAAX motif at the carboxyl terminus.
FTase Inhibitors- Farnesyltransferase inhibitors hold considerable promise as anticancer drugs in the clinical studies. Several studies evaluated including the identification of natural products such as the chaetomellic and zaragozic acids that mimic farnesylpyrophosphate, bisubstrate transition state analogs combining elements of the farnesyl and tetrapeptide substrates and peptidomimetics that reproduce features of the carboxyl terminal tetrapeptide CA1A2X sequence. Several farnesyl transferase inhibitors are in clinical development for the treatment of solid tumors.
FTase inhibitor Emerging Drugs Chapters
This segment of the FTase inhibitor report encloses its detailed analysis of various drugs in different stages of clinical development, including phase III, II, I, preclinical and Discovery. It also helps to understand clinical trial details, expressive pharmacological action, agreements and collaborations, and the latest news and press releases.FTase inhibitor Emerging Drugs
Tipifarnib: Kura Oncology Tipifarnib is an oral investigational farnesyl transferase inhibitor. It is a nonpeptidomimetic quinolinone with potential antineoplastic activity. Tipifarnib binds to and inhibits the enzyme farnesyl protein transferase. By inhibiting the farnesylation of proteins, the molecule prevents the activation of Ras oncogenes, inhibits cell growth, induces apoptosis, and inhibitsangiogenesis.Lonafarnib: Eiger Bio Pharmaceuticals Lonafarnib (also known as SCH66336) is a tricyclic nonpeptidic farnesyl transferase inhibitor that competes with protein substrates for binding to farnesyl transferase. It blocks the post-translational farnesylation of prelamin A and other proteins that are targets for farnesylation. Farnesylation is essential for the function of both mutant and non-mutant lamin-A proteins, including progerin. Merck originally developed Lonafarnib and subsequently licensed it to EigerBiopharmaceuticals.
FTase inhibitor: Therapeutic Assessment
This segment of the report provides insights about the different FTase inhibitor drugs segregated based on following parameters that define the scope of the report, such as:Major Players working on FTase inhibitor
There are approx. 2+ key companies which are developing the FTase inhibitor. The companies which have their FTase inhibitor drug candidates in the most advanced stage, i.e. Phase III include, Eiger Biopharmaceuticals.Phases
This report covers around 2+ products under different phases of clinical development like- Late-stage products (Phase III and
- Mid-stage products (Phase II and
- Early-stage products (Phase I/II and Phase I) along with the details of
- Pre-clinical and Discovery stage candidates
- Discontinued & Inactive candidates
Route of Administration
FTase inhibitor pipeline report provides the therapeutic assessment of the pipeline drugs by the Route of Administration. Products have been categorized under various ROAs such as- Infusion
- Intradermal
- Intramuscular
- Intranasal
- Intravaginal
- Oral
- Parenteral
- Subcutaneous
- Topical.
Molecule Type
Products have been categorized under various Molecule types such as
- Vaccines
- Monoclonal Antibody
- Peptides
- Polymer
- Small molecule
Product Type
Drugs have been categorized under various product types like Mono, Combination and Mono/Combination.FTase inhibitor: Pipeline Development Activities
The report provides insights into different therapeutic candidates in phase II, I, preclinical and discovery stage. It also analyses FTase inhibitor therapeutic drugs key players involved in developing key drugs.Pipeline Development Activities
The report covers the detailed information of collaborations, acquisition and merger, licensing along with a thorough therapeutic assessment of emerging FTase inhibitor drugs.Report Highlights
The companies and academics are working to assess challenges and seek opportunities that could influence FTase inhibitor R&D. The therapies under development are focused on novel approaches for FTase inhibitor.FTase inhibitor Report Insights
- FTASE inhibitor Pipeline Analysis
- Therapeutic Assessment
- Unmet Needs
- Impact of Drugs
FTase inhibitor Report Assessment
- Pipeline Product Profiles
- Therapeutic Assessment
- Pipeline Assessment
- Inactive drugs assessment
- Unmet Needs
Key Questions
Current Scenario and Emerging Therapies:- How many companies are developing FTase inhibitor drugs?
- How many FTase inhibitor drugs are developed by each company?
- How many emerging drugs are in mid-stage, and late-stage of development for FTase inhibitor?
- What are the key collaborations (Industry-Industry, Industry-Academia), Mergers and acquisitions, licensing activities related to the FTase inhibitor therapeutics?
- What are the recent trends, drug types and novel technologies developed to overcome the limitation of existing therapies?
- What are the clinical studies going on for FTase inhibitor and their status?
- What are the key designations that have been granted to the emerging drugs?
Key Players
- Kura Oncology
- Eiger Biopharmaceuticals
Key Products
- Tipifarnib
- Lonafarnib
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Table of Contents
IntroductionExecutive SummaryFTASE inhibitor - Analytical PerspectiveDrug profiles in the detailed report…..Drug profiles in the detailed report…..Drug profiles in the detailed report…..Drug profiles in the detailed report…..FTase inhibitor Key CompaniesFTase inhibitor Key ProductsFTase inhibitor- Unmet NeedsFTase inhibitor- Market Drivers and BarriersFTase inhibitor- Future Perspectives and ConclusionFTase inhibitor Analyst ViewsFTase inhibitor Key CompaniesAppendix
FTASE inhibitor: Overview
Pipeline Therapeutics
Therapeutic Assessment
In-depth Commercial Assessment
FTASE inhibitor Collaboration Deals
Late Stage Products (Phase III)
Tipifarnib: Kura Oncology
Mid Stage Products (Phase II)
Drug name: Company name
Early Stage Products (Phase I)
Drug name: Company name
Pre-clinical and Discovery Stage Products
Drug name: Company name
Inactive Products
List of Tables
List of Figures
Companies Mentioned (Partial List)
A selection of companies mentioned in this report includes, but is not limited to:
- Tipifarnib
- Lonafarnib