Page last updated: 2024-12-05

talactoferrin alfa

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

talactoferrin alfa: recombinant human lactoferrin, an oral drug for treatment of refractory solid tumors; in Phase I trial 5/2006 [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID5619
CHEMBL ID290543
CHEBI ID103981
SCHEMBL ID332192
MeSH IDM0504489

Synonyms (15)

Synonym
BRD-A12822115-003-01-6
L000607
CHEBI:103981
talactoferrin alfa
bdbm86547
cas_135349
nsc_135349
SCHEMBL332192
2-(3,4-dichlorophenyl)-n-methyl-n-[2-(1-pyrrolidinyl)cyclohexyl]acetamide
Q27181219
3,4-dichloro-n-methyl-n-[2-(1-pyrrolidinyl)-cyclohexyl]-benzeneacetamide
CHEMBL290543
149341-39-9
3,4-dichloro-n-methyl-n-[2-(1-pyrrolidinyl)cyclohexyl]benzeneacetamide
DTXSID101155047

Research Excerpts

Overview

Talactoferrin alfa is an oral dendritic cell (DC)-mediated immunotherapy (DCMI) It is a recombinant form of the human glycoprotein, lactoferr in. It has been shown to have a wide range of effects on the immune system.

ExcerptReferenceRelevance
"Talactoferrin alfa is an oral dendritic cell (DC)-mediated immunotherapy (DCMI). "( Talactoferrin alfa versus placebo in patients with refractory advanced non-small-cell lung cancer (FORTIS-M trial).
Barlesi, F; Chang, A; Crawford, J; Douillard, JY; Giaccone, G; Malik, R; Manegold, C; Owonikoko, T; Perez-Soler, R; Pultar, P; Ramalingam, S; Thatcher, N; Wang, Y; Zhu, J, 2013
)
3.28
"Talactoferrin alfa (TLF) is a unique recombinant form of human lactoferrin. "( Immune correlates of talactoferrin alfa in biopsied tumor of relapsed/refractory metastatic non-small cell lung cancer patients.
Bhattacharya, N; Blenman, KR; Engleman, E; Hwang, G; Lee, PP; Malik, R; Neal, JW; Pultar, P; Riess, JW; San-Pedro Salcedo, M; Wakelee, HA, 2014
)
2.16
"Talactoferrin alfa (TLf) is a recombinant human Lf shown to protect against sepsis and necrotizing enterocolitis as well as cancer."( Comparison of bioactivities of talactoferrin and lactoferrins from human and bovine milk.
Du, X; Jiang, R; Lönnerdal, B, 2014
)
1.12
"Talactoferrin alfa is a recombinant form of the human glycoprotein, lactoferrin, which has been shown to have a wide range of effects on the immune system. "( Talactoferrin in Severe Sepsis: Results From the Phase II/III Oral tAlactoferrin in Severe sepsIS Trial.
Dellinger, RP; Guntupalli, K; Levy, MM; Malik, R; Marshall, JC; Simonson, SG; Singer, M; Vincent, JL, 2015
)
1.86

Compound-Compound Interactions

ExcerptReferenceRelevance
"TLF, in combination with C/P, demonstrated an apparent improvement in RR, PFS, and OS in patients with previously untreated stage IIIB/IV non-small cell lung cancer and appears to enhance activity without significant additional toxicity."( A randomized, double-blind, placebo-controlled, phase II study of oral talactoferrin in combination with carboplatin and paclitaxel in previously untreated locally advanced or metastatic non-small cell lung cancer.
Advani, SH; Bapna, A; Digumarti, R; Doval, DC; Julka, PK; Madhavan, J; Malik, R; Nag, S; Parikh, PM; Patil, S; Raman, G; Ranade, AA; Varadhachary, A; Wang, Y, 2011
)
0.37

Dosage Studied

ExcerptRelevanceReference
" Oral TLF or placebo was administered for a maximum of three 14-week cycles with dosing for 12 consecutive weeks followed by 2 weeks off."( Randomized, double-blind, placebo-controlled phase II study of single-agent oral talactoferrin in patients with locally advanced or metastatic non-small-cell lung cancer that progressed after chemotherapy.
Advani, SH; Bapna, A; Digumarti, R; Ismail, PM; Madhavan, J; Malik, R; Nag, S; Parikh, PM; Patil, S; Sekhon, JS; Vaid, A; Varadhachary, A; Wang, Y; Zhu, J, 2011
)
0.37
"Male rats were orally dosed with vehicle or talactoferrin (1000 mg/kg, every day) for 5 d before being subjected to T/HS or trauma-sham shock (T/SS)."( Oral pretreatment with recombinant human lactoferrin limits trauma-hemorrhagic shock-induced gut injury and the biological activity of mesenteric lymph.
Chandler, B; Deitch, EA; Feketova, E; Qin, Y; Quackenbush, EJ; Son, JY, 2014
)
0.4
"These results provide a proof of principle that prophylactic dosing of oral talactoferrin can potentially protect the gut in a T/HS model and limit the production of biologically active factors in rat gastrointestinal tissue subjected to ischemia-reperfusion-type injuries."( Oral pretreatment with recombinant human lactoferrin limits trauma-hemorrhagic shock-induced gut injury and the biological activity of mesenteric lymph.
Chandler, B; Deitch, EA; Feketova, E; Qin, Y; Quackenbush, EJ; Son, JY, 2014
)
0.4
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
acetamidesCompounds with the general formula RNHC(=O)CH3.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Research

Studies (22)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's8 (36.36)29.6817
2010's14 (63.64)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 13.62

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be weak demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index13.62 (24.57)
Research Supply Index3.53 (2.92)
Research Growth Index4.56 (4.65)
Search Engine Demand Index10.37 (26.88)
Search Engine Supply Index4.00 (0.95)

This Compound (13.62)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials10 (43.48%)5.53%
Reviews3 (13.04%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other10 (43.48%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Clinical Trials (7)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
A Phase 2 Randomized, Double-blind, Placebo-controlled Study of the Safety and Efficacy of Talactoferrin Alfa in Patients With Severe Sepsis [NCT00630656]Phase 2190 participants (Actual)Interventional2008-04-30Completed
An Open Label Pilot Study to Evaluate the Effect on the Immune System of Talactoferrin in Adults With Non-Small Cell Lung Cancer (NSCLC) [NCT00923741]Phase 110 participants (Actual)Interventional2008-06-19Completed
Phase 1/2 Study of Talactoferrin Oral Solution for Nosocomial Infection in Preterm Infants [NCT00854633]Phase 1/Phase 2120 participants (Anticipated)Interventional2009-06-30Recruiting
FORTIS-C: A Phase 3, Randomized, Placebo-controlled Study of Oral Talactoferrin in Combination With Carboplatin and Paclitaxel as First-line Therapy in Patients With Locally Advanced or Metastatic Non-small Cell Lung Cancer [NCT00706862]Phase 31,100 participants (Anticipated)Interventional2009-02-28Recruiting
A Phase Ib Immunomodulatory Study of Single Agent Talactoferrin in Patients With Select Relapsed or Refractory Non-Small Cell Lung Cancer (NSCLC) and Squamous Head and Neck Cancer (HNSCC) [NCT01528137]Phase 14 participants (Actual)Interventional2012-05-31Terminated(stopped due to Negative data from another trial led to termination of this trial by sponsor.)
FORTIS-M: A Phase 3, Randomized, Double-blind, Placebo-controlled Study of Oral Talactoferrin in Addition to Best Supportive Care in Patients With Non-small Cell Lung Cancer Who Have Failed Two or More Prior Treatment Regimens [NCT00707304]Phase 3742 participants (Actual)Interventional2008-11-30Completed
OASIS: A Phase 2/3 Randomized, Double-blind, Placebo-controlled Study of the Safety and Efficacy of Talactoferrin Alfa in Patients With Severe Sepsis [NCT01273779]Phase 2/Phase 31,280 participants (Anticipated)Interventional2011-06-30Suspended(stopped due to Data Safety Monitoring Board recommendation)
[information is prepared from clinicaltrials.gov, extracted Sep-2024]