|Trade names||Gleevec, Glivec, others|
|Drug class||Tyrosine kinase inhibitor|
|Metabolism||liver (mainly CYP3A4-mediated)|
|Elimination half-life||18 h (imatinib)|
40 h (active metabolite)
|Excretion||Fecal (68%) and kidney (13%)|
|CompTox Dashboard (EPA)|
|Chemical and physical data|
|Molar mass||493.615 g·mol−1|
|3D model (JSmol)|
Imatinib, sold under the brand name Gleevec among others, is an oral chemotherapy medication used to treat cancer. Specifically, it is used for chronic myelogenous leukemia (CML) and acute lymphocytic leukemia (ALL) that are Philadelphia chromosome-positive (Ph+), certain types of gastrointestinal stromal tumors (GIST), hypereosinophilic syndrome (HES), chronic eosinophilic leukemia (CEL), systemic mastocytosis, and myelodysplastic syndrome. It is taken by mouth.
Common side effects include vomiting, diarrhea, muscle pain, headache, and rash. Severe side effects may include fluid retention, gastrointestinal bleeding, bone marrow suppression, liver problems, and heart failure. Use during pregnancy may result in harm to the baby. Imatinib works by stopping the Bcr-Abl tyrosine-kinase. This can slow growth or result in programmed cell death of certain types of cancer cells.
Imatinib was approved for medical use in the United States in 2001. It is on the World Health Organization's List of Essential Medicines. A generic version became available in the UK as of 2017.
Imatinib is used to treat chronic myelogenous leukemia (CML), gastrointestinal stromal tumors (GISTs) and a number of other malignancies. In 2006 the FDA expended approved use to include Dermatofibrosarcoma protuberans (DFSP), Myelodysplastic/myeloproliferative diseases (MDS/MPD), Aggressive systemic mastocytosis.
Chronic myelogenous leukemia
The U.S. Food and Drug Administration (FDA) has approved imatinib as first-line treatment for Philadelphia chromosome-positive CML, both in adults and children. The drug is approved in multiple contexts of Philadelphia chromosome-positive CML, including after stem cell transplant, in blast crisis, and newly diagnosed.
Gastrointestinal stromal tumors
The FDA first granted approval for advanced GIST patients in 2002. On 1 February 2012, imatinib was approved for use after the surgical removal of KIT-positive tumors to help prevent recurrence. The drug is also approved in unresectable KIT-positive GISTs.
The FDA granted approval for the treatment of DFSP patients in 2006. Specifically adult patients with unresectable, recurrent and/or metastatic dermatofibrosarcoma protuberans (DFSP). Prior to approval DFSP was considered unresponsive to chemotherapy treatments.
The FDA has approved imatinib for use in adults with relapsed or refractory Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ ALL), myelodysplastic/ myeloproliferative diseases associated with platelet-derived growth factor receptor gene rearrangements, aggressive systemic mastocytosis without or an unknown D816V c-KIT mutation, hypereosinophilic syndrome and/or chronic eosinophilic leukemia who have the FIP1L1-PDGFRα fusion kinase (CHIC2 allele deletion) or FIP1L1-PDGFRα fusion kinase negative or unknown, unresectable, recurrent and/or metastatic dermatofibrosarcoma protuberans. On 25 January 2013, Gleevec was approved for use in children with Ph+ ALL.
For treatment of progressive plexiform neurofibromas associated with neurofibromatosis type I, early research has shown potential for using the c-KIT tyrosine kinase blocking properties of imatinib.
Contraindications and cautions
- Hepatic impairment
- Risk of severe CHF or left ventricular dysfunction, especially in patients with comorbidities
- Pregnancy, risk of embryo-fetal toxicity
- Risk of fluid retention
- Risk of growth stunting in children or adolescents
The most common side effects include nausea, vomiting, diarrhea, headaches, leg aches/cramps, fluid retention, visual disturbances, itchy rash, lowered resistance to infection, bruising or bleeding, loss of appetite; weight gain, reduced number of blood cells (neutropenia, thrombocytopenia, anemia), and edema. Although rare, restoration of hair color has been reported as well. Severe congestive cardiac failure is an uncommon but recognized side effect of imatinib and mice treated with large doses of imatinib show toxic damage to their myocardium.
Mechanism of action
|Therapeutic use||chronic myelogenous leukemia|
|Biological target||ABL, c-kit, PDGF-R|
|Mechanism of action||Tyrosine-kinase inhibitor|
|PDB ligand id||STI:,|
There are a large number of TK enzymes in the body, including the insulin receptor. Imatinib is specific for the TK domain in abl (the Abelson proto-oncogene), c-kit and PDGF-R (platelet-derived growth factor receptor).
In chronic myelogenous leukemia, the Philadelphia chromosome leads to a fusion protein of abl with bcr (breakpoint cluster region), termed bcr-abl. As this is now a constitutively active tyrosine kinase, imatinib is used to decrease bcr-abl activity.
The active sites of tyrosine kinases each have a binding site for ATP. The enzymatic activity catalyzed by a tyrosine kinase is the transfer of the terminal phosphate from ATP to tyrosine residues on its substrates, a process known as protein tyrosine phosphorylation. Imatinib works by binding close to the ATP binding site of bcr-abl, locking it in a closed or self-inhibited conformation, and therefore inhibiting the enzyme activity of the protein semi-competitively. This fact explains why many BCR-ABL mutations can cause resistance to imatinib by shifting its equilibrium toward the open or active conformation.
Imatinib is quite selective for bcr-abl, though it does also inhibit other targets mentioned above (c-kit and PDGF-R), as well as ABL2 (ARG) and DDR1 tyrosine kinases and NQO2 – an oxidoreductase. Imatinib also inhibits the abl protein of non-cancer cells, but these cells normally have additional redundant tyrosine kinases, which allows them to continue to function even if abl tyrosine kinase is inhibited. Some tumor cells, however, have a dependence on bcr-abl. Inhibition of the bcr-abl tyrosine kinase also stimulates its entry in to the nucleus, where it is unable to perform any of its normal anti-apoptopic functions, leading to tumor cell death.
Other pathways affected
The Bcr-Abl pathway has many downstream pathways including
- the Ras/MapK pathway, which leads to increased proliferation due to increased growth factor-independent cell growth.
- It also affects the Src/Pax/Fak/Rac pathway. This affects the cytoskeleton, which leads to increased cell motility and decreased adhesion.
- The PI/PI3K/AKT/BCL-2 pathway is also affected. BCL-2 is responsible for keeping the mitochondria stable; this suppresses cell death by apoptosis and increases survival.
- The last pathway that Bcr-Abl affects is the JAK/STAT pathway, which is responsible for proliferation.
Imatinib is rapidly absorbed when given by mouth, and is highly bioavailable: 98% of an oral dose reaches the bloodstream. Metabolism of imatinib occurs in the liver and is mediated by several isozymes of the cytochrome P450 system, including CYP3A4 and, to a lesser extent, CYP1A2, CYP2D6, CYP2C9, and CYP2C19. The main metabolite, N-demethylated piperazine derivative, is also active. The major route of elimination is in the bile and feces; only a small portion of the drug is excreted in the urine. Most of imatinib is eliminated as metabolites; only 25% is eliminated unchanged. The half-lives of imatinib and its main metabolite are 18 h and 40 h, respectively. It blocks the activity of Abelson cytoplasmic tyrosine kinase (ABL), c-Kit and the platelet-derived growth factor receptor (PDGFR). As an inhibitor of PDGFR, imatinib mesylate appears to have utility in the treatment of a variety of dermatological diseases. Imatinib has been reported to be an effective treatment for FIP1L1-PDGFRalpha+ mast cell disease, hypereosinophilic syndrome, and dermatofibrosarcoma protuberans.
Its use is advised against in people on strong CYP3A4 inhibitors such as clarithromycin, chloramphenicol, ketoconazole, ritonavir and nefazodone due to its reliance on CYP3A4 for metabolism. Likewise it is a CYP3A4, CYP2D6 and CYP2C9 inhibitor and hence concurrent treatment with substrates of any of these enzymes may increase plasma concentrations of said drugs. Since imatinib is mainly metabolised via the liver enzyme CYP3A4, substances influencing the activity of this enzyme change the plasma concentration of the drug. An example of a drug that increases imatinib activity and therefore side effects by blocking CYP3A4 is ketoconazole. The same could be true of itraconazole, clarithromycin, grapefruit juice, among others. Conversely, CYP3A4 inductors like rifampicin and St John's Wort reduce the drug's activity, risking therapy failure. Imatinib also acts as an inhibitor of CYP3A4, 2C9 and 2D6, increasing the plasma concentrations of a number of other drugs like simvastatin, ciclosporin, pimozide, warfarin, metoprolol, and possibly paracetamol. The drug also reduces plasma levels of levothyroxin via an unknown mechanism.
As with other immunosuppressants, application of live vaccines is contraindicated because the microorganisms in the vaccine could multiply and infect the patient. Inactivated and toxoid vaccines do not hold this risk, but may not be effective under imatinib therapy.
Imatinib was invented in the late 1990s by scientists at Ciba-Geigy (which merged with Sandoz in 1996 to become Novartis), in a team led by biochemist Nicholas Lydon and that included Elisabeth Buchdunger and Jürg Zimmermann and its use to treat CML was driven by oncologist Brian Druker of Oregon Health & Science University (OHSU). Other major contributions to imatinib development were made by Carlo Gambacorti-Passerini, a physician, scientist, and hematologist at University of Milano Bicocca, Italy, John Goldman at Hammersmith Hospital in London, UK, and later on by Charles Sawyers of Memorial Sloan-Kettering Cancer Center.
Imatinib was developed by rational drug design. After the Philadelphia chromosome mutation and hyperactive bcr-abl protein were discovered, the investigators screened chemical libraries to find a drug that would inhibit that protein. With high-throughput screening, they identified 2-phenylaminopyrimidine. This lead compound was then tested and modified by the introduction of methyl and benzamide groups to give it enhanced binding properties, resulting in imatinib.
When Novartis tested imatinib in rats, mice, rabbits, dogs, and monkeys in 1996, it was found to have several toxic effects; in particular, results indicating liver damage in dogs nearly stopped drug development completely. However, favorable results in studies with monkeys and in vitro human cells allowed testing to continue in humans.
The first clinical trial of Gleevec took place in 1998, after Novartis reluctantly synthesized and released a few grams of the drug for Druker, enough for him to run a trial using a hundred or so patients. The drug received FDA approval in May 2001, only two and a half years after the new drug application was submitted. On the same month it made the cover of TIME magazine as a "bullet" to be used against cancer. Druker, Lydon and Sawyers received the Lasker-DeBakey Clinical Medical Research Award in 2009 for "converting a fatal cancer into a manageable chronic condition".
A Swiss patent application was filed on imatinib and various salts on in April 1992, which was then filed in the EU, the US, and other countries in March and April 1993. and in 1996 United States and European patent offices issued patents listing Jürg Zimmermann as the inventor.
In July 1997, Novartis filed a new patent application in Switzerland on the beta crystalline form of imatinib mesylate (the mesylate salt of imatinib). The "beta crystalline form" of the molecule is a specific polymorph of imatinib mesylate; a specific way that the individual molecules pack together to form a solid. This is the actual form of the drug sold as Gleevec/Glivec; a salt (imatinib mesylate) as opposed to a free base, and the beta crystalline form as opposed to the alpha or other form.:3 and 4 In 1998, Novartis filed international patent applications claiming priority to the 1997 filing. A United States patent was granted in 2005.
Society and culture
In 2013, more than 100 cancer specialists published a letter in Blood saying that the prices of many new cancer drugs, including imatinib, are so high that people in the United States couldn't afford them, and that the level of prices, and profits, was so high as to be immoral. Signatories of the letter included Brian Druker, Carlo Gambacorti-Passerini, and John Goldman, developers of imatinib. They wrote that in 2001, imatinib was priced at $30,000 (equivalent to $43,317 in 2019) a year, which was based on the price of interferon, then the standard treatment, and that at this price Novartis would have recouped its initial development costs in two years. They wrote that after unexpectedly becoming a blockbuster, Novartis increased the price to $92,000 (equivalent to $102,455 in 2019) per year in 2012, with annual revenues of $4.7 billion. Other physicians have complained about the cost.
Druker himself, who led the clinical studies, never got a patent and never made money from it.
By 2016, the average wholesale price had increased to $120,000 (equivalent to $127,837 in 2019) a year, according to an analysis prepared for The Washington Post by Stacie Dusetzina of the University of North Carolina at Chapel Hill. When competitive drugs came on the market, they were sold at a higher price to reflect the smaller population,[clarification needed] and Novartis raised the price of Gleevec to match them.
A 2012 economic analysis funded by Bristol-Myers Squibb estimated that the discovery and development of imatinib and related drugs had created $143 billion in societal value at a cost to consumers of approximately $14 billion. The $143 billion figure was based on an estimated 7.5 to 17.5 year survival advantage conferred by imatinib treatment, and included the value (discounted at 3% per annum) of ongoing benefits to society after the imatinib patent expiration.
Patent litigation in India
Novartis fought a seven-year, controversial battle to patent Gleevec in India, and took the case all the way to the Indian Supreme Court. The patent application at the center of the case was filed by Novartis in India in 1998, after India had agreed to enter the World Trade Organization and to abide by worldwide intellectual property standards under the TRIPS agreement. As part of this agreement, India made changes to its patent law, the biggest of which was that prior to these changes, patents on products were not allowed, while afterwards they were, albeit with restrictions. These changes came into effect in 2005, so Novartis' patent application waited in a "mailbox" with others until then, under procedures that India instituted to manage the transition. India also passed certain amendments to its patent law in 2005, just before the laws came into effect.
The patent application claimed the final form of Gleevec (the beta crystalline form of imatinib mesylate).:3 In 1993, during the time India did not allow patents on products, Novartis had patented imatinib, with salts vaguely specified, in many countries but could not patent it in India. The key differences between the two patent applications, were that 1998 patent application specified the counterion (Gleevec is a specific salt – imatinib mesylate) while the 1993 patent application did not claim any specific salts nor did it mention mesylate, and the 1998 patent application specified the solid form of Gleevec – the way the individual molecules are packed together into a solid when the drug itself is manufactured (this is separate from processes by which the drug itself is formulated into pills or capsules) – while the 1993 patent application did not. The solid form of imatinib mesylate in Gleevec is beta crystalline.
As provided under the TRIPS agreement, Novartis applied for Exclusive Marketing Rights (EMR) for Gleevec from the Indian Patent Office and the EMR was granted in November 2003. Novartis made use of the EMR to obtain orders against some generic manufacturers who had already launched Gleevec in India.
When examination of Novartis' patent application began in 2005, it came under immediate attack from oppositions initiated by generic companies that were already selling Gleevec in India and by advocacy groups. The application was rejected by the patent office and by an appeal board. The key basis for the rejection was the part of Indian patent law that was created by amendment in 2005, describing the patentability of new uses for known drugs and modifications of known drugs. That section, 3d, specified that such inventions are patentable only if "they differ significantly in properties with regard to efficacy." At one point, Novartis went to court to try to invalidate Section 3d; it argued that the provision was unconstitutionally vague and that it violated TRIPS. Novartis lost that case and did not appeal. Novartis did appeal the rejection by the patent office to India's Supreme Court, which took the case.
The Supreme Court case hinged on the interpretation of Section 3d. The Supreme Court issued its decision in 2013, ruling that the substance that Novartis sought to patent was indeed a modification of a known drug (the raw form of imatinib, which was publicly disclosed in the 1993 patent application and in scientific articles), that Novartis did not present evidence of a difference in therapeutic efficacy between the final form of Gleevec and the raw form of imatinib, and that therefore the patent application was properly rejected by the patent office and lower courts.
One study demonstrated that imatinib mesylate was effective in patients with systemic mastocytosis, including those who had the D816V mutation in c-KIT. However, since imatinib binds to tyrosine kinases when they are in the inactive configuration and the D816V mutant of c-KIT is constitutively active, imatinib does not inhibit the kinase activity of the D816V mutant of c-KIT. Experience has shown, however, that imatinib is much less effective in patients with this mutation, and patients with the mutation comprise nearly 90% of cases of mastocytosis.
Imatinib was initially thought to have a potential role in the treatment of pulmonary hypertension. It was shown to reduce both the smooth muscle hypertrophy and hyperplasia of the pulmonary vasculature in a variety of disease processes, including portopulmonary hypertension. However, a long-term trial of Imatinib in people with pulmonary arterial hypertension was unsuccessful, and serious and unexpected adverse events were frequent. These included 6 subdural hematomas and 17 deaths during or within 30 days of study end.
In systemic sclerosis, the drug has been tested for potential use in slowing down pulmonary fibrosis. In laboratory settings, imatinib is being used as an experimental agent to suppress platelet-derived growth factor (PDGF) by inhibiting its receptor (PDGF-Rβ). One of its effects is delaying atherosclerosis in mice without or with diabetes.
In vitro studies identified that a modified version of imatinib can bind to gamma-secretase activating protein (GSAP). GSAP selectively increases the production and accumulation of neurotoxic beta-amyloid plaques, which suggests that molecules which target GSAP and are able to cross blood–brain barrier are potential therapeutic agents for treating Alzheimer's disease. Another study suggests that imatinib may not need to cross the blood–brain barrier to be effective at treating Alzheimer's, as the research indicates the production of beta-amyloid may begin in the liver. Tests on mice indicate that imatinib is effective at reducing beta-amyloid in the brain. It is not known whether reduction of beta-amyloid is a feasible way of treating Alzheimer's, as an anti-beta-amyloid vaccine has been shown to clear the brain of plaques without having any effect on Alzheimer symptoms.
A formulation of imatinib with a cyclodextrin (Captisol) as a carrier to overcome the blood–brain barrier is also currently[when?] considered as an experimental drug for lowering and reversing opioid tolerance.[medical citation needed] Imatinib has shown reversal of tolerance in rats. Imatinib is an experimental drug in the treatment of desmoid tumor or aggressive fibromatosis.[medical citation needed]
- "Imatinib (Gleevec) Use During Pregnancy". Drugs.com. 27 August 2018. Retrieved 16 February 2020.
- "Imatinib Mesylate". The American Society of Health-System Pharmacists. Archived from the original on 16 January 2017. Retrieved 8 January 2017.
- World Health Organization (2019). World Health Organization model list of essential medicines: 21st list 2019. Geneva: World Health Organization. hdl:10665/325771. WHO/MVP/EMP/IAU/2019.06. License: CC BY-NC-SA 3.0 IGO.
- "Oxford Pharmacy Store Generic Imatinib : Oxford Pharmacy Store". oxfordpharmacystore.co.uk. Archived from the original on 2 April 2017. Retrieved 1 April 2017.
- "Gleevec Gains Simultaneous FDA Approval for Five Rare, Life-Threatening Disorders". Cancer Network. 1 November 2006. Retrieved 10 June 2020.
- "FDA Highlights and Prescribing Information for Gleevec(imatinib mesylate)" (PDF). Archived (PDF) from the original on 13 September 2014.
- "Leukemia – Chronic Myeloid – CML: Statistics | Cancer.Net". 26 June 2012. Archived from the original on 12 November 2014.
- "Cancer Stat Facts: Leukemia — Chronic Myeloid Leukemia (CML)". Cancer.gov. Retrieved 17 April 2020.
- "Prolonged Use of Imatinib in GIST Patients Leads to New FDA Approval". Archived from the original on 4 February 2012.
- "FDA approves Gleevec for children with acute lymphoblastic leukemia". FDA News Release. US Food and Drug Administration. 25 January 2013. Archived from the original on 10 March 2013. Retrieved 3 April 2013.
- Yang FC, Ingram DA, Chen S, Zhu Y, Yuan J, Li X, Yang X, Knowles S, Horn W, Li Y, Zhang S, Yang Y, Vakili ST, Yu M, Burns D, Robertson K, Hutchins G, Parada LF, Clapp DW (October 2008). "Nf1-dependent tumors require a microenvironment containing Nf1+/--and c-kit-dependent bone marrow". Cell. 135 (3): 437–48. doi:10.1016/j.cell.2008.08.041. PMC 2788814. PMID 18984156. Lay summary – Science Daily.
- "Gleevec NF1 Trial". Nfcure.org. Archived from the original on 20 April 2012. Retrieved 3 April 2013.
- "GIST in Neurofibromatosis 1". Gistsupport.org. 14 May 2010. Archived from the original on 29 March 2013. Retrieved 3 April 2013.
- ""Pilot Study of Gleevec/Imatinib Mesylate (STI-571, NSC 716051) in Neurofibromatosis (NF1) Patient With Plexiform Neurofibromas (0908-09)" (Suspended)". Clinicaltrials.gov. Archived from the original on 3 July 2013. Retrieved 3 April 2013.
- "Glivec Tablets – Summary of Product Characteristics (SPC)". electronic Medicines Compendium. Novartis Pharmaceuticals UK Ltd. Archived from the original on 1 February 2014.
- "Gleevec (imatinib) dosing, indications, interactions, adverse effects, and more". Medscape Reference. WebMD. Archived from the original on 3 January 2014. Retrieved 24 January 2014.
- "Imatinib". Macmillan Cancer Support. Archived from the original on 22 November 2012. Retrieved 26 December 2012.
- Haberfeld, H, ed. (2009). Austria-Codex (in German) (2009/2010 ed.). Vienna: Österreichischer Apothekerverlag. ISBN 978-3-85200-196-8.
- Altman, Lawrence K. (8 August 2002). "Leukemia Drug Side Effect: Color Returned to Gray Hair". The New York Times. Archived from the original on 8 December 2015. Retrieved 5 December 2015.
In a puzzling and intriguing side effect, a new antileukemia drug has darkened the gray hair of some patients, French doctors reported yesterday.
- "Cancer drug restores hair colour". BBC News Online. 8 August 2002. Archived from the original on 26 September 2015. Retrieved 5 December 2015.
A drug developed to treat leukaemia has been found to have surprising side effect - it appears able to restore colour to grey hair.
- Kerkelä R, Grazette L, Yacobi R, Iliescu C, Patten R, Beahm C, Walters B, Shevtsov S, Pesant S, Clubb FJ, Rosenzweig A, Salomon RN, Van Etten RA, Alroy J, Durand JB, Force T (August 2006). "Cardiotoxicity of the cancer therapeutic agent imatinib mesylate". Nat. Med. 12 (8): 908–16. doi:10.1038/nm1446. PMID 16862153. S2CID 9385835.
- Shima H, Tokuyama M, Tanizawa A, Tono C, Hamamoto K, Muramatsu H, Watanabe A, Hotta N, Ito M, Kurosawa H, Kato K, Tsurusawa M, Horibe K, Shimada H (October 2011). "Distinct impact of imatinib on growth at prepubertal and pubertal ages of children with chronic myeloid leukemia". J. Pediatr. 159 (4): 676–81. doi:10.1016/j.jpeds.2011.03.046. PMID 21592517.
- "Glivec (imatinib)" (PDF). TGA eBusiness Services. Novartis Pharmaceuticals Australia Pty Ltd. 21 August 2013. Archived from the original on 12 January 2017. Retrieved 24 January 2014.
- "Crystal structures of the kinase domain of c-Abl in complex with the small molecule inhibitors PD173955 and imatinib (STI-571)" (PDF). Cancer Res. 62 (15): 4236–43. PMID 12154025. ; Nagar B, Bornmann WG, Pellicena P, Schindler T, Veach DR, Miller WT, Clarkson B, Kuriyan J (August 2002).
- Takimoto CH, Calvo E. "Principles of Oncologic Pharmacotherapy" Archived 15 May 2009 at the Wayback Machine in Pazdur R, Wagman LD, Camphausen KA, Hoskins WJ (Eds)Cancer Management: A Multidisciplinary Approach Archived 4 October 2013 at the Wayback Machine. 11 ed. 2008.
- Gambacorti-Passerini CB, Gunby RH, Piazza R, Galietta A, Rostagno R, Scapozza L (February 2003). "Molecular mechanisms of resistance to imatinib in Philadelphia-chromosome-positive leukaemias". Lancet Oncol. 4 (2): 75–85. doi:10.1016/S1470-2045(03)00979-3. PMID 12573349.
- Hantschel, Oliver; Rix, Uwe; Superti-Furga, Giulio (1 January 2008). "Target spectrum of the BCR-ABL inhibitors imatinib, nilotinib and dasatinib". Leukemia & Lymphoma. 49 (4): 615–619. doi:10.1080/10428190801896103. ISSN 1042-8194. PMID 18398720. S2CID 33895941.
- Deininger MW, Druker BJ (September 2003). "Specific targeted therapy of chronic myelogenous leukemia with imatinib". Pharmacol. Rev. 55 (3): 401–23. doi:10.1124/pr.55.3.4. PMID 12869662. S2CID 8620208.
- Vigneri P, Wang JY (February 2001). "Induction of apoptosis in chronic myelogenous leukemia cells through nuclear entrapment of BCR-ABL tyrosine kinase". Nat. Med. 7 (2): 228–34. doi:10.1038/84683. PMID 11175855. S2CID 40934433.
- Weisberg E, Manley PW, Cowan-Jacob SW, Hochhaus A, Griffin JD (May 2007). "Second generation inhibitors of BCR-ABL for the treatment of imatinib-resistant chronic myeloid leukaemia". Nature Reviews Cancer. 7 (5): 345–56. doi:10.1038/nrc2126. PMID 17457302. S2CID 20640317.
- Scheinfeld N, Schienfeld N (February 2006). "A comprehensive review of imatinib mesylate (Gleevec) for dermatological diseases". J Drugs Dermatol. 5 (2): 117–22. PMID 16485879.
- Klopp, T, ed. (2010). Arzneimittel-Interaktionen (in German) (2010/2011 ed.). Arbeitsgemeinschaft für Pharmazeutische Information. ISBN 978-3-85200-207-1.
- Staff, Innovation.org (a project of the Pharmaceutical Research and Manufacturers of America)The Story of Gleevec Archived 21 October 2013 at the Wayback Machine
- Dreifus, Claudia (2 November 2009). "Researcher Behind the Drug Gleevec". The New York Times. Archived from the original on 14 January 2014. Retrieved 16 February 2020.
- Gambacorti-Passerini C (June 2008). "Part I: Milestones in personalised medicine--imatinib". Lancet Oncology. 9 (6): 600. doi:10.1016/S1470-2045(08)70152-9. PMID 18510992.
- Druker BJ, Lydon NB (January 2000). "Lessons learned from the development of an abl tyrosine kinase inhibitor for chronic myelogenous leukemia". J. Clin. Invest. 105 (1): 3–7. doi:10.1172/JCI9083. PMC 382593. PMID 10619854.
- Pippin, J. J. (2012). "Animal research in medical sciences: Seeking a convergence of science, medicine, and animal law". S. Tex. L. Rev. 54: 469. Archived from the original on 18 September 2017..
- Monmaney, Terence (3 December 1999). "A Triumph in the War Against Cancer". Smithsonian. Retrieved 16 January 2017.
- Li, J.J. (2015). Top Drugs: History, Pharmacology, Syntheses. Oxford University Press. p. 81. ISBN 978-0-19-936259-2. Archived from the original on 18 September 2017.
- Siddhartha, Mukherjee (2010). The Emperor of All Maladies. New York, NY: Scribner. pp. 436. ISBN 978-1-4391-0795-9.
- Novartis press release, 10 May 2001. FDA approves Novartis' unique cancer medication Glivec
- Cohen MH et al. Approval Summary for Imatinib Mesylate Capsules in the Treatment of Chronic Myelogenous Leukemia Archived 19 July 2012 at the Wayback Machine Clin Cancer Res May 2002 8; 935
- Margot J. Fromer for Oncology Times. December 2002. What's in a Name? Quite a Lot When It Comes to Marketing & Selling New Cancer Drugs Archived 21 October 2013 at the Wayback Machine
- Novartis Press Release. 30 April 2001 Novartis Oncology Changes Trade Name of Investigational Agent Glivec to Gleevec in the United States
- U.S. Patent 5,521,184
- "Imatinib Patent Family". Espacenet. 1996. Retrieved 23 July 2014.
- EP 0564409
- Staff, European Medicines Agency, 2004.EMEA Scientific Discussion of Glivec Archived 5 November 2014 at the Wayback Machine
- Note: The Indian patent application, which became the subject of litigation in India that gathered a lot of press, does not appear to be publicly available. However according to documents produced in the course of that litigation Archived 16 July 2015 at the Wayback Machine (page 27), "The Appellant's application under the PCT was substantially on the same invention as had been made in India."
- WO 9903854
- U.S. Patent 6,894,051
- Experts in Chronic Myeloid Leukemia (May 2013). "The price of drugs for chronic myeloid leukemia (CML) is a reflection of the unsustainable prices of cancer drugs: from the perspective of a large group of CML experts". Blood. 121 (22): 4439–42. doi:10.1182/blood-2013-03-490003. PMC 4190613. PMID 23620577. Archived from the original on 26 March 2014.
- Pollack, Andrew (25 April 2013). "Doctors Denounce Cancer Drug Prices of $100,000 a Year". The New York Times. Archived from the original on 21 February 2017. Retrieved 16 February 2020.
- Schiffer CA (July 2007). "BCR-ABL tyrosine kinase inhibitors for chronic myelogenous leukemia". N. Engl. J. Med. 357 (3): 258–65. doi:10.1056/NEJMct071828. PMID 17634461.
- Pollack, Andrew (14 April 2009). "As Pills Treat Cancer, Insurance Lags Behind". The New York Times. Archived from the original on 2 November 2014. Retrieved 16 February 2020.
- Brody, Jane E. (18 January 2010). "Living With a Formerly Fatal Blood Cancer". The New York Times. Archived from the original on 9 February 2017. Retrieved 16 February 2020.
- Rosenthal, Elisabeth (21 June 2018). "Why Competition Won't Bring Down Drug Prices". The New York Times. Retrieved 16 February 2020.
- "This drug is defying a rare form of leukemia — and it keeps getting pricier". The Washington Post. 9 March 2016. Archived from the original on 10 March 2016. Retrieved 10 March 2016.
- Yin W, Penrod JR, Maclean R, Lakdawalla DN, Philipson T (November 2012). "Value of survival gains in chronic myeloid leukemia". Am J Manag Care. 18 (11 Suppl): S257–64. PMID 23327457. Archived from the original on 24 July 2015.
- Patented Medicine Review Board (Canada). Archived 6 July 2011 at the Wayback Machine Report on New Patented Drugs – Gleevec.
- "pharmacychecker.com". pharmacychecker.com. Archived from the original on 2 February 2014. Retrieved 3 April 2013.
- Harris, Gardiner; Thomas, Katie (1 April 2013). "Low-Cost Drugs in Poor Nations Get a Lift in Indian Court". The New York Times. Archived from the original on 20 December 2014. Retrieved 16 February 2020.
- "The Novartis Patent Case: The Full Supreme Court Ruling". The New York Times. 1 April 2013. Retrieved 16 February 2020.
- Note: The Indian patent application No.1602/MAS/1998 does not appear to be publicly available. However according to the decision of the IPAB on 26 June 2009 Archived 16 July 2015 at the Wayback Machine (page 27) discussed below, "The Appellant's application under the PCT was substantially on the same invention as had been made in India."
- Staff, European Medicines Agency, 2004. EMEA Scientific Discussion of Glivec Archived 5 November 2014 at the Wayback Machine
- Indian Supreme Court Decision Archived 6 July 2013 at the Wayback Machine paragraphs 5–6
- Novartis v UoI, para 8–9 Archived 6 July 2013 at the Wayback Machine
- Shamnad Basheer for Spicy IP 11 March 2006 First Mailbox Opposition (Gleevec) Decided in India Archived 21 October 2013 at the Wayback Machine
- R. Jai Krishna and Jeanne Whalen for the Wall Street Journal. 1 April 2013 Novartis Loses Glivec Patent Battle in India Archived 29 May 2016 at the Wayback Machine
- Intellectual Property Appellate Board decision dated 26 June 2009, p 149 Archived 16 July 2015 at the Wayback Machine
- W.P. No.24759 of 2006 Archived 20 October 2013 at the Wayback Machine
- "Supreme Court rejects bid by Novartis to patent Glivec". Archived from the original on 17 December 2013.
- Droogendijk HJ, Kluin-Nelemans HJ, van Doormaal JJ, Oranje AP, van de Loosdrecht AA, van Daele PL (July 2006). "Imatinib mesylate in the treatment of systemic mastocytosis: a phase II trial". Cancer. 107 (2): 345–51. doi:10.1002/cncr.21996. PMID 16779792. S2CID 41124956.
- Tapper EB, Knowles D, Heffron T, Lawrence EC, Csete M (June 2009). "Portopulmonary hypertension: imatinib as a novel treatment and the Emory experience with this condition". Transplant. Proc. 41 (5): 1969–71. doi:10.1016/j.transproceed.2009.02.100. PMID 19545770.
- Frost, Adaani E.; Barst, Robyn J.; Hoeper, Marius M.; Chang, Hyuk-Jae; Frantz, Robert P.; Fukumoto, Yoshihiro; Galié, Nazzareno; Hassoun, Paul M.; Klose, Hans (2015). "Long-term safety and efficacy of imatinib in pulmonary arterial hypertension". The Journal of Heart and Lung Transplantation. 34 (11): 1366–1375. doi:10.1016/j.healun.2015.05.025. PMID 26210752.
- Boucher P, Gotthardt M, Li WP, Anderson RG, Herz J (April 2003). "LRP: role in vascular wall integrity and protection from atherosclerosis". Science. 300 (5617): 329–32. Bibcode:2003Sci...300..329B. doi:10.1126/science.1082095. PMID 12690199. S2CID 2070128.
- Lassila M, Allen TJ, Cao Z, Thallas V, Jandeleit-Dahm KA, Candido R, Cooper ME (May 2004). "Imatinib attenuates diabetes-associated atherosclerosis". Arterioscler. Thromb. Vasc. Biol. 24 (5): 935–42. doi:10.1161/01.ATV.0000124105.39900.db. PMID 14988091.
- Reeves PM, Bommarius B, Lebeis S, McNulty S, Christensen J, Swimm A, Chahroudi A, Chavan R, Feinberg MB, Veach D, Bornmann W, Sherman M, Kalman D (July 2005). "Disabling poxvirus pathogenesis by inhibition of Abl-family tyrosine kinases". Nat. Med. 11 (7): 731–9. doi:10.1038/nm1265. PMID 15980865. S2CID 28325503.
- He G, Luo W, Li P, Remmers C, Netzer WJ, Hendrick J, Bettayeb K, Flajolet M, Gorelick F, Wennogle LP, Greengard P (September 2010). "Gamma-secretase activating protein is a therapeutic target for Alzheimer's disease". Nature. 467 (7311): 95–8. Bibcode:2010Natur.467...95H. doi:10.1038/nature09325. PMC 2936959. PMID 20811458.
- "Alzheimer's may start in liver – Health – Alzheimer's Disease | NBC News". NBC News. 8 March 2011. Retrieved 6 January 2013.
- Holmes C, Boche D, Wilkinson D, Yadegarfar G, Hopkins V, Bayer A, Jones RW, Bullock R, Love S, Neal JW, Zotova E, Nicoll JA (July 2008). "Long-term effects of Abeta42 immunisation in Alzheimer's disease: follow-up of a randomised, placebo-controlled phase I trial". Lancet. 372 (9634): 216–23. doi:10.1016/S0140-6736(08)61075-2. PMID 18640458. S2CID 18340153.
- Eliminating Morphine Tolerance – Reformulated Imatinib Archived 29 March 2013 at the Wayback Machine 23 Feb 2012, 5:00 PST