primaquine has been researched along with Inborn Errors of Metabolism in 17 studies
Primaquine: An aminoquinoline that is given by mouth to produce a radical cure and prevent relapse of vivax and ovale malarias following treatment with a blood schizontocide. It has also been used to prevent transmission of falciparum malaria by those returning to areas where there is a potential for re-introduction of malaria. Adverse effects include anemias and GI disturbances. (From Martindale, The Extra Pharmacopeia, 30th ed, p404)
primaquine : An N-substituted diamine that is pentane-1,4-diamine substituted by a 6-methoxyquinolin-8-yl group at the N(4) position. It is a drug used in the treatment of malaria and Pneumocystis pneumonia.
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 16 (94.12) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 1 (5.88) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Bennett, JW | 1 |
Pybus, BS | 1 |
Yadava, A | 1 |
Tosh, D | 1 |
Sousa, JC | 1 |
McCarthy, WF | 1 |
Deye, G | 1 |
Melendez, V | 1 |
Ockenhouse, CF | 1 |
PORTER, IH | 1 |
BARNARD, DR | 1 |
JACOB, HS | 1 |
INGBAR, SH | 1 |
JANDL, JH | 1 |
Vermorken, AJ | 1 |
Weterings, PJ | 1 |
de Bruyn, CH | 1 |
Geerts, SJ | 1 |
Frischer, H | 1 |
Carson, PE | 1 |
Vesell, ES | 1 |
Waller, HD | 1 |
La Du, BN | 1 |
Yawata, Y | 1 |
Kjellstrand, C | 1 |
Buselmeier, T | 1 |
Howe, R | 1 |
Jacob, H | 1 |
Waldenström, JG | 1 |
Gaetani, GF | 1 |
Garré, C | 1 |
Ajmar, F | 1 |
Bianchi, GL | 1 |
Sunahara, S | 1 |
Beutler, E | 1 |
Panizon, F | 1 |
Cohen, RJ | 1 |
Sachs, JR | 1 |
Wicker, DJ | 1 |
Conrad, ME | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
Safety, Tolerability and Pharmacokinetics of Tafenoquine After Weekly and Escalating Monthly Doses of Tafenoquine in Healthy Vietnamese Volunteers[NCT05203744] | Phase 4 | 200 participants (Anticipated) | Interventional | 2022-05-10 | Not yet recruiting | ||
A Clinical Study to Assess the Safety and Feasibility of Controlled Blood-stage Plasmodium Vivax Human Malaria Infection Through Experimental Inoculation of Cryopreserved Infected Erythrocytes in Healthy Thai Adults[NCT05071079] | 16 participants (Anticipated) | Interventional | 2022-05-23 | Recruiting | |||
Phase 1/2a Open-label Dose Safety, Reactogenicity, Immunogenicity and Efficacy of the Candidate Plasmodium Vivax Malaria Protein 001 (VMP001) Administered Intramuscularly With GlaxoSmithKline (GSK) Biologicals' Adjuvant System AS01B in Healthy Malaria-Naï[NCT01157897] | Phase 1/Phase 2 | 41 participants (Actual) | Interventional | 2010-07-31 | Completed | ||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
"Subjects were ranked according to time of onset of parasitemia and a non-parametric rankorder statistical test (eg, Log-Rank or Mann-Whitney) was performed to evaluate delays in parasitemia induced by vaccination. Cox Proportional Hazards model was used to calculate days to parasitemia and Kaplan-Meier plots were used to display time to first positive malaria blood smear.~Hazard Ratio (HR). Time starts once subject has received t infectious bites. Time stops when subject has first positive blood smear. If subject does not become parasitemic then time stops the day he/she begins anti-malarial therapy." (NCT01157897)
Timeframe: 280 day (during the study through 6 months aftr challenge)
Intervention | days (Mean) |
---|---|
Cohort 1: 15 μg VMP001 | 0.137 |
Cohort 2: 30 μg VMP001 | 0.073 |
Cohort 3: 60 μg VMP001 | 0.042 |
Anti-VMP001 antibody concentrations were measured and summarized by geometric mean titers (GMT) with 95% confidence interval (CI). Peak responses were compared by performing Student's t-test on data normalized by log transformation to ascertain the presence or absence of significant dose response differences. ELISA Units (EU) were converted to log10 values for calculations and statistical comparison of geometric means. Units that were reported as '>50' were converted to '1'. (NCT01157897)
Timeframe: study duration
Intervention | Geometric Mean Titier of European Units (Mean) | |||||||
---|---|---|---|---|---|---|---|---|
Pre-vaccination | 2wks post first vaccination | Day of second vaccination | 2wks post second vaccination | Day of third vaccination | 2wks post third vaccination | 4wks post challenge | 6mths post challenge | |
Cohort 1: 15 μg VMP001 | 1 | 133.72 | 244.35 | 20161.18 | 9053.32 | 61203.48 | 54843.38 | 10860.7 |
Cohort 2: 30 μg VMP001 | 1 | 750.38 | 1450.22 | 81143.72 | 31071.01 | 68730.4 | 56472.17 | 12519.16 |
Cohort 3: 60 μg VMP001 | 3.09 | 836.68 | 1711.63 | 61711.8 | 36405.66 | 41879.99 | 32178.39 | 5500.73 |
Anti-VMP001 antibody concentrations were measured and summarized by geometric mean titers (GMT) with 95% confidence interval (CI). Peak responses were compared by performing Student's t-test on data normalized by log transformation to ascertain the presence or absence of significant dose response differences. ELISA Units (EU) were converted to log10 values for calculations and statistical comparison of geometric means. Units that were reported as '>50' were converted to '1'. (NCT01157897)
Timeframe: study duration
Intervention | Geometric Mean Titer of European Units (Mean) | |||||||
---|---|---|---|---|---|---|---|---|
Pre-vaccination | 2wks post first vaccination | Day of second vaccination | 2wks post second vaccination | Day of third vaccination | 2wks post third vaccination | 4wks post challenge | 6months post challenge | |
Cohort 1: 15 μg VMP001 | 1 | 151.39 | 281.79 | 21862.22 | 9921.61 | 59883.77 | 54843.38 | 10860.7 |
Cohort 2: 30 μg VMP001 | 1.5 | 526.18 | 1175.41 | 74608.62 | 28498.43 | 68730.4 | 56472.17 | 12519.16 |
Cohort 3: 60 μg VMP001 | 3.09 | 836.68 | 1711.63 | 61711.8 | 36405.66 | 41879.99 | 32178.39 | 5500.73 |
Adverse events were evaluated for 7 days after each vaccination during the vaccine phase. (NCT01157897)
Timeframe: 7 days after immunization
Intervention | participants with AEs (Number) | ||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|
Solicited Local: Injection site erythema | Solicited Local: Injection site induration | Solicited Local: Injection site pain | Solicited Systemic: Diarrhea | Solicited Systemic: Nausea | Solicited Systemic: Vomiting | Solicited Systemic: Fatigue | Solicited Systemic: Pyrexia | Solicited Systemic: Arthralgia | Solicited Systemic: Myalgia | Solicited Systemic: Headache | |
Cohort 1: 15 μg VMP001 | 2 | 0 | 10 | 0 | 5 | 2 | 8 | 4 | 4 | 4 | 8 |
Cohort 2: 30 μg VMP001 | 3 | 1 | 10 | 0 | 3 | 0 | 4 | 2 | 2 | 4 | 6 |
Cohort 3: 60 μg VMP001 | 6 | 2 | 10 | 1 | 4 | 2 | 7 | 1 | 3 | 7 | 5 |
Adverse events were evaluated over a 28 day follow-up period after each vaccination during the vaccine phase (NCT01157897)
Timeframe: 28 days following immunization
Intervention | participants with AEs (Number) | ||||||||||||||||||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Ear discomfort | Abdominal discomfort | Abdominal pain | Feces discolored | Food poisoning | Nausea | Toothache | Axillary pain | Chills | Feeling hot | Injection site erythema | Injection site pruritus | Injection site swelling | Injection site warmth | Malaise | Hypertransaminasaemia | Seasonal allergy | Nasopharyngitis | Upper respiratory tract infection | Contusion | Excoriation | Postprocedural discomfort | Posttraumatic pain | Scratch | Skin laceration | Haemoglobin decreased | Platelet count decreased | Gout | Back pain | Muscle spasms | Musculoskeletal discomfort | Myalgia | Pain in extremity | Dizziness | Headache | Sinus headache | Nasal Congestion | Cold sweat | Dermatitis contact | Erythema | Hypertension | |
Cohort 1: 15 μg VMP001 | 1 | 1 | 0 | 0 | 1 | 1 | 2 | 0 | 5 | 5 | 0 | 0 | 0 | 0 | 3 | 1 | 1 | 1 | 2 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | 1 | 1 | 1 | 2 | 1 | 1 | 0 | 0 | 2 | 0 | 0 | 1 |
Cohort 2: 30 μg VMP001 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 5 | 6 | 0 | 0 | 2 | 1 | 5 | 2 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | 1 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 4 | 1 | 1 | 0 |
Cohort 3: 60 μg VMP001 | 0 | 0 | 1 | 1 | 0 | 0 | 0 | 0 | 7 | 7 | 1 | 1 | 3 | 2 | 7 | 1 | 1 | 0 | 2 | 1 | 1 | 0 | 1 | 1 | 2 | 1 | 1 | 0 | 1 | 0 | 1 | 0 | 2 | 1 | 0 | 1 | 1 | 2 | 0 | 0 | 0 |
6 reviews available for primaquine and Inborn Errors of Metabolism
Article | Year |
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GENETIC BASIS OF DRUG METABOLISM IN MAN.
Topics: Barbiturates; Catalase; Drug Tolerance; Genetics, Medical; Humans; Isoniazid; Metabolism; Metabolism | 1964 |
ENZYME DEFECTS IN THE HUMAN RED CELL.
Topics: Anemia; Blood Protein Disorders; Drug Therapy; Enzymes; Erythrocytes; Favism; Hemoglobinuria; Hemogl | 1964 |
Recent progress in pharmacogenetics.
Topics: Adult; Aged; Alcohol Oxidoreductases; Antipyrine; Asian People; Child, Preschool; Cholinesterases; C | 1969 |
[Adverse effects of drugs in hereditary variants in the enzyme apparatus of the body].
Topics: Adenosine Triphosphatases; Adult; Aged; Cholinesterase Inhibitors; Coumarins; Dibucaine; Drug-Relate | 1968 |
Genetic determimants in drug action.
Topics: Acetylation; Acetyltransferases; Cholinesterases; Coumarins; Dealkylation; Drug Resistance; Genes; G | 1972 |
[Drug reactions and human genetics].
Topics: Asian People; Black People; Catalase; Cholinesterases; Genetics, Medical; Humans; Isoniazid; Metabol | 1967 |
1 trial available for primaquine and Inborn Errors of Metabolism
Article | Year |
---|---|
Primaquine failure and cytochrome P-450 2D6 in Plasmodium vivax malaria.
Topics: Adolescent; Adult; Cytochrome P-450 CYP2D6; Female; Humans; Malaria, Vivax; Male; Metabolism, Inborn | 2013 |
Primaquine failure and cytochrome P-450 2D6 in Plasmodium vivax malaria.
Topics: Adolescent; Adult; Cytochrome P-450 CYP2D6; Female; Humans; Malaria, Vivax; Male; Metabolism, Inborn | 2013 |
Primaquine failure and cytochrome P-450 2D6 in Plasmodium vivax malaria.
Topics: Adolescent; Adult; Cytochrome P-450 CYP2D6; Female; Humans; Malaria, Vivax; Male; Metabolism, Inborn | 2013 |
Primaquine failure and cytochrome P-450 2D6 in Plasmodium vivax malaria.
Topics: Adolescent; Adult; Cytochrome P-450 CYP2D6; Female; Humans; Malaria, Vivax; Male; Metabolism, Inborn | 2013 |
Primaquine failure and cytochrome P-450 2D6 in Plasmodium vivax malaria.
Topics: Adolescent; Adult; Cytochrome P-450 CYP2D6; Female; Humans; Malaria, Vivax; Male; Metabolism, Inborn | 2013 |
Primaquine failure and cytochrome P-450 2D6 in Plasmodium vivax malaria.
Topics: Adolescent; Adult; Cytochrome P-450 CYP2D6; Female; Humans; Malaria, Vivax; Male; Metabolism, Inborn | 2013 |
Primaquine failure and cytochrome P-450 2D6 in Plasmodium vivax malaria.
Topics: Adolescent; Adult; Cytochrome P-450 CYP2D6; Female; Humans; Malaria, Vivax; Male; Metabolism, Inborn | 2013 |
Primaquine failure and cytochrome P-450 2D6 in Plasmodium vivax malaria.
Topics: Adolescent; Adult; Cytochrome P-450 CYP2D6; Female; Humans; Malaria, Vivax; Male; Metabolism, Inborn | 2013 |
Primaquine failure and cytochrome P-450 2D6 in Plasmodium vivax malaria.
Topics: Adolescent; Adult; Cytochrome P-450 CYP2D6; Female; Humans; Malaria, Vivax; Male; Metabolism, Inborn | 2013 |
10 other studies available for primaquine and Inborn Errors of Metabolism
Article | Year |
---|---|
OXIDATIVE HEMOLYSIS AND ERYTHROCYTE METABOLISM IN HEREDITARY ACATALASIA.
Topics: Acatalasia; Anemia; Anemia, Hemolytic; Ascorbic Acid; Azides; Catalase; Cyanides; Erythrocyte Aging; | 1965 |
Human hair follicles in biomedical research.
Topics: Acne Vulgaris; Female; Genotype; Glucose Dehydrogenases; Hair; Humans; Metabolism, Inborn Errors; Pr | 1981 |
Multiple gene interactions in pharmacogenetics.
Topics: Animals; Erythrocyte Aging; Glucosephosphate Dehydrogenase Deficiency; Humans; Hydroxylation; Metabo | 1981 |
Hemolysis in dialyzed patients: tap water-induced red blood cell metabolic deficiency.
Topics: Anemia, Hemolytic; Ascorbic Acid; Carbon Radioisotopes; Cell Survival; Chromium Radioisotopes; Eryth | 1972 |
Editorial: Pharmacogenetics.
Topics: Drug Interactions; Enzymes; Glucosephosphate Dehydrogenase; Humans; Isoniazid; Metabolism, Inborn Er | 1973 |
Influence of riboflavin and of erythrocyte stroma on glutathione reductase activity in normal, glucose 6 phosphate dehydrogenase deficient and low glutathione reductase individuals.
Topics: Cell Membrane; Clinical Enzyme Tests; Deficiency Diseases; Drug Interactions; Enzyme Activation; Ery | 1973 |
Abnormalities of the hexose monophosphate shunt.
Topics: Anemia, Hemolytic; Black People; Blood Transfusion; Chromium Isotopes; Dihydrolipoamide Dehydrogenas | 1971 |
[Pathogenesis of favism].
Topics: Anemia, Hemolytic; Diagnosis, Differential; Favism; Glucosephosphate Dehydrogenase Deficiency; Human | 1967 |
Methemoglobinemia provoked by malarial chemoprophylaxis in Vietnam.
Topics: Antimalarials; Chloroquine; Cyanosis; Dapsone; Diseases in Twins; Erythrocytes; Female; Hematocrit; | 1968 |
Hemolytic anemia complicating viral hepatitis and G-6-PD deficiency.
Topics: Anemia, Hemolytic; Anemia, Hemolytic, Congenital; Aspirin; Glucosephosphate Dehydrogenase Deficiency | 1969 |