Ancestim
Identification
- Summary
Ancestim is a human stem cell factor used in combination with filgrastim during autologous peripheral blood progenitor cell (PBPC) transplantation to increase PBPC mobilization for improved collection.
- Generic Name
- Ancestim
- DrugBank Accession Number
- DB09103
- Background
Ancestim is a non-glycosylated recombinant methionyl human stem cell factor. It is a 166 amino acid protein produced by E. coli with an amino acid sequence that is identical to the natural sequence predicted from human DNA sequence analysis, except for the addition of an N-terminal methionine5. Ancestim was developed by Amgen and sold to Biovitrium in December 2008. It was submitted to the FDA under the status of recommendation for approval with a 10 to 1 votes.2 It was also approved by Health Canada in 1999 but it is currently under the status of canceled post-market.4
- Type
- Biotech
- Groups
- Approved, Investigational, Withdrawn
- Biologic Classification
- Protein Based Therapies
Haematopoietic growth factors - Protein Structure
- Protein Chemical Formula
- C1662H2650N422O512S18
- Protein Average Weight
- 18540.0 Da (non-glycosylated)
- Sequences
>>Sequence Stem Cell Factor<<<< MEGICRNRVTNNVKDVTKLVANLPKDYMITLKYVPGMDVLPSHCWISEMVVQLSDSLTDL LDKFSNISEGLSNYSIIDKLVNIVDDLVECVKENSSKDLKKSFKSPEPRLFTPEEFFRIF NRSIDAFKDFVVASETSDCVVSSTLSPEKDSRVSVTKPFMLPPVA
Download FASTA Format- Synonyms
- Ancestim
Pharmacology
- Indication
Ancestim, in combination with filgrastim, is indicated for the setting of autologous peripheral blood progenitor cell transplantation in patients at risk of poor peripheral blood progenitor cell mobilisation.7 The use of ancestim with filgrastim will generate a sustained increase in the number of peripheral blood progenitor cells capable of engraftment. It is used for mobilization of progenitor cells from the bone marrow to the peripheral blood with or withouth mobilizing chemotherapy. The harvested progenitor cells can be used for transplant following myelosuppressive or myeloablative therapies.6
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- Pharmacodynamics
Ancestim action on hemotopeitic progenitor cells stimulates its proliferation, differentiation, commitment and functional activation. This stimulation results in an increase on circulating peripheral blood progenitor cells like CD34, granulocyte macrophage colony-forming units and erythroid burst-forming units.6
- Mechanism of action
Ancestim alone is unable to increase peripheral blood progenitor cells so it has to be administered with filgastrim, a granulocyte colony-stimulating factor.3 Ancestrim will bind to the c-KIT expressed in hemocytoblasts, myeloid progenitors, megakaryocytes, immature mast cells, myeloblasts and lymphoid progenitors. Ancestim binding will cause receptor homodimerization and autophosphorylation at tyrosine residues. The activation of this receptor leads to the activation of a signaling cascade that contains the RAS/ERK, PI3-Kinase, Src kinase and JAK/STAT pathways which will later stimulate proliferation, differentiation and activation of the cell lines.1
Target Actions Organism AMast/stem cell growth factor receptor Kit agonistHumans - Absorption
The pharmacokinetics of ancestim has a dose-linear profile. After subcutaneous administration, ancestim has an absorption half-life of 35-41 hours following a mean lag of 2 hours. When a dose of 5-25 mcg/kg is administered, the peak concentration of 3.6-13.7 ng/ml is reached after 15-24 hours. In preclinical studies, the bioavailability of ancestim was reported to be greater than 60%. After multiple dosing, the steady state was reached after 4-5 days from the beginning of the treatment.6
- Volume of distribution
Preclinical reports demonstrate that after intravenous administration of ancestim, the distribution profile is primarily in plasma and kidneys with a subsequent and rapid loss from all tissues.6
- Protein binding
Not Available
- Metabolism
Administration of ancestim in preclinical trials have proven that from the excreted dose all of it is formed by degraded ancestim into lower molecular weigth products.6
- Route of elimination
In preclinical studies, it was shown that 90% of the administered dose is excreted in the urine.6
- Half-life
In clinical trials, the reported half life for ancestim was between 2-5 hours.6
- Clearance
The apparent clearance reported for ancestim is approximately 35-40 ml/h/kg.6
- Adverse Effects
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- Toxicity
Ancestim was not genotoxic for gene mutation or chromosomal damage and it did not have any effect in fertility.6
- Pathways
- Not Available
- Pharmacogenomic Effects/ADRs
- Not Available
Interactions
- Drug Interactions
- This information should not be interpreted without the help of a healthcare provider. If you believe you are experiencing an interaction, contact a healthcare provider immediately. The absence of an interaction does not necessarily mean no interactions exist.
Drug Interaction Integrate drug-drug
interactions in your softwareAbacavir Abacavir may decrease the excretion rate of Ancestim which could result in a higher serum level. Aceclofenac Aceclofenac may decrease the excretion rate of Ancestim which could result in a higher serum level. Acemetacin Acemetacin may decrease the excretion rate of Ancestim which could result in a higher serum level. Acetaminophen Acetaminophen may decrease the excretion rate of Ancestim which could result in a higher serum level. Acetazolamide Acetazolamide may increase the excretion rate of Ancestim which could result in a lower serum level and potentially a reduction in efficacy. Acetylsalicylic acid Acetylsalicylic acid may decrease the excretion rate of Ancestim which could result in a higher serum level. Aclidinium Aclidinium may decrease the excretion rate of Ancestim which could result in a higher serum level. Acrivastine Ancestim may decrease the excretion rate of Acrivastine which could result in a higher serum level. Acyclovir Acyclovir may decrease the excretion rate of Ancestim which could result in a higher serum level. Adefovir dipivoxil Adefovir dipivoxil may decrease the excretion rate of Ancestim which could result in a higher serum level. Identify potential medication risksEasily compare up to 40 drugs with our drug interaction checker.Get severity rating, description, and management advice.Learn more - Food Interactions
- Not Available
Products
- Drug product information from 10+ global regionsOur datasets provide approved product information including:dosage, form, labeller, route of administration, and marketing period.Access drug product information from over 10 global regions.
- Mixture Products
Name Ingredients Dosage Route Labeller Marketing Start Marketing End Region Image Stemgen Ancestim (1875 mcg / vial) + Water (5 mL / vial) Kit; Powder, for solution Subcutaneous Biovitrum Ab (Publ) 1999-09-20 2012-12-31 Canada Stemgen Ancestim (2500 mcg / vial) + Water (5 mL / vial) Kit; Powder, for solution Subcutaneous Biovitrum Ab (Publ) Not applicable Not applicable Canada
Categories
- ATC Codes
- L03AA12 — Ancestim
- Drug Categories
- Chemical TaxonomyProvided by Classyfire
- Description
- Not Available
- Kingdom
- Organic Compounds
- Super Class
- Organic Acids
- Class
- Carboxylic Acids and Derivatives
- Sub Class
- Amino Acids, Peptides, and Analogues
- Direct Parent
- Peptides
- Alternative Parents
- Not Available
- Substituents
- Not Available
- Molecular Framework
- Not Available
- External Descriptors
- Not Available
- Affected organisms
- Humans and other mammals
Chemical Identifiers
- UNII
- PYB4Q6JG41
- CAS number
- 163545-26-4
References
- General References
- Ronnstrand L: Signal transduction via the stem cell factor receptor/c-Kit. Cell Mol Life Sci. 2004 Oct;61(19-20):2535-48. doi: 10.1007/s00018-004-4189-6. [Article]
- Trahan P. (1999). Clinical Handbook for biotherapy. Jones and Bartlett Publishers Inc..
- Galbraith A., Bullock S., Manias E., Hunt B., and Richards A. (2013). Fundamentals of Pharmacology: An applied approach for nursing and health (2nd ed.). Pearson Education Limited. [ISBN:1741031443]
- Health Canada [Link]
- Sobi [Link]
- Stemgen monograph [Link]
- Stemgen monograph [Link]
- External Links
- MSDS
- Download (133 KB)
Clinical Trials
- Clinical Trials
Phase Status Purpose Conditions Count 2 Completed Treatment Multiple Myeloma (MM) 1 0 Unknown Status Treatment Myelodysplastic Syndrome 1
Pharmacoeconomics
- Manufacturers
- Not Available
- Packagers
- Not Available
- Dosage Forms
Form Route Strength Kit; powder, for solution Subcutaneous - Prices
- Not Available
- Patents
- Not Available
Properties
- State
- Solid
- Experimental Properties
Property Value Source melting point (°C) 230ºC 'MSDS' boiling point (°C) 520ºC at 760 mmHg 'MSDS' water solubility Insoluble 'MSDS' isoelectric point 5.86 'MSDS'
Targets

- Kind
- Protein
- Organism
- Humans
- Pharmacological action
- Yes
- Actions
- Agonist
- General Function
- Transmembrane receptor protein tyrosine kinase activity
- Specific Function
- Tyrosine-protein kinase that acts as cell-surface receptor for the cytokine KITLG/SCF and plays an essential role in the regulation of cell survival and proliferation, hematopoiesis, stem cell main...
- Gene Name
- KIT
- Uniprot ID
- P10721
- Uniprot Name
- Mast/stem cell growth factor receptor Kit
- Molecular Weight
- 109863.655 Da
References
Drug created at September 16, 2015 22:07 / Updated at January 14, 2023 19:02