Evaluation of Solanidine as an Exogenous Biomarker to Phenotype CYP2D6 Activity in Humans (SOLA-1)
This study investigates the evaluation of solanidine as an exogenous biomarker to phenotype CYP2D6-activity in humans. Participants will be classified by their CYP2D6 genotype into poor metabolizers (PM), low intermediate metabolizers (LIM), extensive metabolizers (EM) and ultra-rapid metabolizers (UM), forming four distinct study arms:
Arm 1) Poor Metabolizers (PM) n=10 Arm 2) Low Intermediate Metabolizers (LIM) n=5 Arm 3) Extensive Metabolizers (EM) n=10 Arm 4) Ultra-rapid Metabolizers (UM) n=5
Participants will be given a standardized potato-rich meal, serving as the natural source of solanidine, and will be phenotyped for CYP2D6 activity with a single oral microdose of the probe drug yohimbine.
The objectives of the study are as follows:
- To evaluate the suitability of the SSDA/solanidine and m414/solanidine metabolic ratio as an exogenous biomarker to phenotype CYP2D6 activity in humans.
- To characterize the postprandial plasma concentration profile of solanidine, its CYP2D6-dependent metabolites, and its parent molecules α-solanine and α-chaconine following a potato-rich meal.
Studieöversikt
Status
Betingelser
Intervention / Behandling
Detaljerad beskrivning
The study follows an open-label, controlled, parallel-cohort design with four study arms based on CYP2D6 genotype. The study consists of two parts: a Yohimbine and a Potato Part.
Yohimbine Part:
Participants will receive a single oral microdose of 50 μg of yohimbine, administered in a fasted state as 2 x 1 tablets of Yohimbinum hydrochloricum D4® (Deutsche Homöopathie Union, Karlsruhe, Germany, containing 25 μg per tablet). A total of 6 blood samples will be collected at defined time points (baseline; 10; 20; 30; 60; 120 min). At each time point, 5 mL of blood will be drawn for plasma separation to determine yohimbine and the primary metabolite 11-OH-yohimbine. The blood sampling protocol is based on the findings of the YOKI-1 study (protocol number: IPHA-2025-011, Greifswald Ethics Committee Registration number BB 069/25). At baseline, an additional blood sample will be collected for a random determination of solanidine and its metabolites. During the 2.5-hour stay in the CRU, participants will be asked to stay in bed.
Potato Part:
Between the Potato and the Yohimbine Part, a period of 4 weeks in any order is acceptable. The Potato Part is divided into two sequential phases: Phase 1 and Phase 2, both featuring supervised meal ingestion at the clincal research unit. During the three days before each Potato Phase and up to 60 hours afterward, no potato products should be eaten. Otherwise, ad libitum food intake is permitted beginning six hours after the potato-rich meal. Blood samples will be analyzed for solanidine, its CYP2D6-dependent metabolites, and its parent molecules α-solanine and α-chaconine in both Potato Phases. Both Potato Phases must be separated by at least one week.
Phase 1 (0-12 hours postprandial):
An initial baseline blood sample will be collected prior to the ingestion of the potato-rich meal. Participants will receive the potato-rich meal at 8 a.m., and a total of 7 blood samples will be collected at defined time points (baseline, 2, 4, 6, 8, 10, and 12 h).Upon successful completion of the 12-hour blood draw, participants will be discharged from the CRU.
Phase 2 (12-60 hours postprandial):
On a separate scheduled study day, participants will report to the CRU at 7:30 p.m. A baseline blood sample will be collected prior to meal ingestion. Participants will then ingest an identical, defined potato-rich meal at 8:00 p.m. Following meal consumption, participants are permitted to go home for the night. The next morning, starting at 7:30 a.m., blood sampling collections will begin at the designated time points. A total of ten blood samples will be collected at defined time points (baseline, 12, 14, 16, 18, 20, 22, 24 h, 36 h in the next morning and at 60 h in the morning thereafter).
Studietyp
Inskrivning (Beräknad)
Fas
- Inte tillämpbar
Kontakter och platser
Studiekontakt
- Namn: Stefan Engeli, Prof. Dr.
- Telefonnummer: +49 3834 86 5633
- E-post: stefan.engeli@med.uni-greifswald.de
Studieorter
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Mecklenburg-Vorpommern
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Greifswald, Mecklenburg-Vorpommern, Tyskland, 17489
- University Medicine Greifswald
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Kontakt:
- Stefan Engeli, Prof. Dr.
- Telefonnummer: +49 3834 86 5633
- E-post: stefan.engeli@med.uni-greifswald.de
-
Huvudutredare:
- Stefan Engeli, Prof. Dr.
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Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
- Vuxen
Tar emot friska volontärer
Beskrivning
Inclusion Criteria:
- individuals of both biological sexes, assigned as women or men at birth
- age: ≥ 18 and ≤ 40 years
- possesses the ability to understand the study purpose and design
- contractually capable and provides signed informed consent form
- in good general health or with mild and/or well-managed conditions such as allergies, asthma, hypertension or orthopedic diseases
- taking no more than three chronic medications
- ability to maintain and record a detailed dietary protocol focusing on the consumption of potato-based products for the specified duration of the study
- individuals classified as either ultrarapid metabolizers (UM), extensive metabolizers (EM), low intermediate metabolizers (LIM) or poor metabolizers (PM) based on their CYP2D6 genotype:
Poor Metabolizer (PM, Gen-Score 0):
homozygous or compound heterozygous for CYP2D6 *3, CYP2D6 *4, CYP2D6*5, CYP2D6 *6
Low Intermediate Metabolizer (LIM, Gen-Score 0,25 or 0,5):
Homozygous or compound heterozygous for CYP2D6 *9, *10, *41 or compound heterozygous with one allele of CYP2D6 *3, CYP2D6 *4, CYP2D6*5, or CYP2D6*6 and one allele of CYP2D6 *17 (0,5) or CYP2D6 *9, *10, or *41 (0,25)
Extensive Metabolizer (EM, Gene-Score 2):
homozygous or compound heterozygous for CYP2D6 *1, CYP2D6 *2, CYP2D6*35
Ultrarapid Metabolizer (UM, Gen-Score ≥ 3):
homozygous or compound heterozygous for CYP2D6 *1, CYP2D6 *2, CYP2D6*35 with at least one allele duplicated or multiplied
Exclusion Criteria:
- BMI > 30 kg/m2 and < 18 kg/m2
- body weight < 48 kg
- women: known pregnancy or lactation period; positive urine pregnancy test at screening or kinetic visit
- men: hemoglobin < 13 g/dl (8,07 mmol/l) women: hemoglobin < 12 g/dl (7,45 mmol/l)
- elevated liver function tests (1 or more of ALAT, ASAT, yGT, Bilirubin > 2x ULN)
- reduced renal function (eGFRMDRD < 60 mL/min/1,7 m2)
- QTcF > 450 ms in screening ECG
- current or recent psychiatric disorders requiring treatment including depression, bipolar disorder, schizophrenia, psychosis or severe anxiety disorders
- drug dependency at the time of visit
- use of recreational drugs more than twice a week
- intake of drugs interfering with CYP2D6 during the past seven days
- any known hypersensitivity or allergic reactions to yohimbine
- intake of yohimbine within 48 hours prior to study participation
- history of hypersensitivity or allergy to potatoes or nightshade vegetables
- intake of potato-containing meals during the three days before and after eating the potato-rich test meal
- history of severe hypersensitivity reactions and/or anaphylaxis
- poor venous conditions that make it impossible to place a peripheral venous catheter and regularly draw blood through it
- engagement in extreme physical activity within 48 hours prior to study participation
Studieplan
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Grundläggande vetenskap
- Tilldelning: Icke-randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
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Aktiv komparator: Poor Metabolizers (PM):
Participants in this arm are classified as poor metabolizers (PM, Gene-Score 0) based on their CYP2D6 genotype.
Poor metabolizers are homozygous or compound heterozygous for CYP2D6 *3, CYP2D6 *4, CYP2D6 *5, CYP2D6 *6.
Participants were selected to achieve best matching between arms according to age, BMI, alcohol consumption and smoking.
|
A single oral dose of 50 µg yohimbine, administered as 2 x 1 tablets of Yohimbinum hydrochloricum D4® will be administered as drinking solution with 240mL of water under overnight fasting conditions.
A total of 6 blood samples will be collected at defined time points (baseline; 10; 20; 30; 60; 120 min).
At each time point, 5 mL of blood will be drawn for plasma separation to determine yohimbine and the primary metabolite 11-OH-yohimbine.
Potato Intervention (2 phases): Diet restriction: No potato products 3 days before and until 60h after each meal. Ad libitum food intake is allowed from 6h post-meal. Blood will be analyzed for solanidine, its metabolites and its parent molecules α-solanine, and α-chaconine. Phase 1 (0-12h postprandial): Baseline blood draw at 8:00 AM, followed by supervised ingestion of a potato-rich meal. A total of 7 blood samples will be collected (baseline, 2, 4, 6, 8, 10, 12h) before discharge from the CRU. Phase 2 (12-60h postprandial): Baseline blood draw at 7:30 PM, identical meal ingestion at 8:00 PM. Participants can go home afterwards and return to the CRU the next morning at 8:00 AM for their 12 hour post meal blood draw. A total of 10 blood samples will be collected (baseline, 12, 14, 16, 18, 20, 22, 24h, 36h next morning, 60h subsequent morning).
Andra namn:
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Aktiv komparator: Low Intermediate Metabolizer (LIM)
Low intermediae metabolizers (LIM, Gene-Score 0,25 or 0,5) are homozygous or compound heterozygous for CYP2D6 *9, *10, *41 or compound heterozygous with one allele of CYP2D6 *3, CYP2D6 *4, CYP2D6*5, or CYP2D6 *6 and one allele of CYP2D6 *17 (0,5) or CYP2D6 *9, *10, or *41 (0,25).
Participants were selected to achieve best matching between arms according to age, BMI, alcohol consumption and smoking.
|
A single oral dose of 50 µg yohimbine, administered as 2 x 1 tablets of Yohimbinum hydrochloricum D4® will be administered as drinking solution with 240mL of water under overnight fasting conditions.
A total of 6 blood samples will be collected at defined time points (baseline; 10; 20; 30; 60; 120 min).
At each time point, 5 mL of blood will be drawn for plasma separation to determine yohimbine and the primary metabolite 11-OH-yohimbine.
Potato Intervention (2 phases): Diet restriction: No potato products 3 days before and until 60h after each meal. Ad libitum food intake is allowed from 6h post-meal. Blood will be analyzed for solanidine, its metabolites and its parent molecules α-solanine, and α-chaconine. Phase 1 (0-12h postprandial): Baseline blood draw at 8:00 AM, followed by supervised ingestion of a potato-rich meal. A total of 7 blood samples will be collected (baseline, 2, 4, 6, 8, 10, 12h) before discharge from the CRU. Phase 2 (12-60h postprandial): Baseline blood draw at 7:30 PM, identical meal ingestion at 8:00 PM. Participants can go home afterwards and return to the CRU the next morning at 8:00 AM for their 12 hour post meal blood draw. A total of 10 blood samples will be collected (baseline, 12, 14, 16, 18, 20, 22, 24h, 36h next morning, 60h subsequent morning).
Andra namn:
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Aktiv komparator: Extensive Metabolizer (EM)
Extensive Metabolizer (EM, Gene-Score 2) are homozygous or compound heterozygous for CYP2D6 *1, CYP2D6 *2, CYP2D6*35.
Participants were selected to achieve best matching between arms according to age, BMI, alcohol consumption and smoking.
|
A single oral dose of 50 µg yohimbine, administered as 2 x 1 tablets of Yohimbinum hydrochloricum D4® will be administered as drinking solution with 240mL of water under overnight fasting conditions.
A total of 6 blood samples will be collected at defined time points (baseline; 10; 20; 30; 60; 120 min).
At each time point, 5 mL of blood will be drawn for plasma separation to determine yohimbine and the primary metabolite 11-OH-yohimbine.
Potato Intervention (2 phases): Diet restriction: No potato products 3 days before and until 60h after each meal. Ad libitum food intake is allowed from 6h post-meal. Blood will be analyzed for solanidine, its metabolites and its parent molecules α-solanine, and α-chaconine. Phase 1 (0-12h postprandial): Baseline blood draw at 8:00 AM, followed by supervised ingestion of a potato-rich meal. A total of 7 blood samples will be collected (baseline, 2, 4, 6, 8, 10, 12h) before discharge from the CRU. Phase 2 (12-60h postprandial): Baseline blood draw at 7:30 PM, identical meal ingestion at 8:00 PM. Participants can go home afterwards and return to the CRU the next morning at 8:00 AM for their 12 hour post meal blood draw. A total of 10 blood samples will be collected (baseline, 12, 14, 16, 18, 20, 22, 24h, 36h next morning, 60h subsequent morning).
Andra namn:
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Aktiv komparator: Ultrarapid Metabolizer
Ultrarapid Metabolizer (UM, Gen-Score ≥ 3) are homozygous or compound heterozygous for CYP2D6 *1, CYP2D6 *2, CYP2D6*35 with at least one allele duplicated or multiplied.
Participants were selected to achieve best matching between arms according to age, BMI, alcohol consumption and smoking.
|
A single oral dose of 50 µg yohimbine, administered as 2 x 1 tablets of Yohimbinum hydrochloricum D4® will be administered as drinking solution with 240mL of water under overnight fasting conditions.
A total of 6 blood samples will be collected at defined time points (baseline; 10; 20; 30; 60; 120 min).
At each time point, 5 mL of blood will be drawn for plasma separation to determine yohimbine and the primary metabolite 11-OH-yohimbine.
Potato Intervention (2 phases): Diet restriction: No potato products 3 days before and until 60h after each meal. Ad libitum food intake is allowed from 6h post-meal. Blood will be analyzed for solanidine, its metabolites and its parent molecules α-solanine, and α-chaconine. Phase 1 (0-12h postprandial): Baseline blood draw at 8:00 AM, followed by supervised ingestion of a potato-rich meal. A total of 7 blood samples will be collected (baseline, 2, 4, 6, 8, 10, 12h) before discharge from the CRU. Phase 2 (12-60h postprandial): Baseline blood draw at 7:30 PM, identical meal ingestion at 8:00 PM. Participants can go home afterwards and return to the CRU the next morning at 8:00 AM for their 12 hour post meal blood draw. A total of 10 blood samples will be collected (baseline, 12, 14, 16, 18, 20, 22, 24h, 36h next morning, 60h subsequent morning).
Andra namn:
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Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
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Metabolic ratio of SSDA/solanidine
Tidsram: From enrollment to 60 hours after eating the potato-rich meal.
|
This study determines the sensitivity of the metabolic ratio of SSDA/solanidine and the metabolic ratio of m414/solanidine to correctly identify the CYP2D6 metabolizer status.
Each MR will be considered separately in order to identify the most suitable one.
As we will recruit individuals from the lowest and highest level of CYP2D6 activity, we will test the sensitivity independently for the prediction of the lowest activity level (PM + LIM) and the highest activity level (EM + UM).
The "true" CYP2D6 metabolizer status will be determined by the combination of the CYP2D6 genotype and the yohimbine-determined phenotype in recruited individuals.
Those individuals with a perfect match of genotype and phenotype are considered the controls to which the solanidine results are then compared as the ratio of phenotype predicted (by solandine MR)/ phenotype determined (by genotyping + yohimbine-phenotyping)
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From enrollment to 60 hours after eating the potato-rich meal.
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Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
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AUC for solanidine, SSDA, m414, α-solanine and α-chaconine
Tidsram: 60 hours
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Plasma concentrations expressed as area under the curve (AUC) will be determined for solanidine, its CYP2D6-dependent metabolites SSDA and m414, and its parent molecules α-solanine and α-chaconine for each metabolizer status cohort (PM, LIM, EM, UM).
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60 hours
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Cmax for solanidine, SSDA, m414, α-solanine and α-chaconine
Tidsram: 60 hours
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The maximum concentration (Cmax) will be determined for solanidine, its CYP2D6-dependent metabolites SSDA and m414, and its parent molecules α-solanine and α-chaconine for each metabolizer status cohort (PM, LIM, EM, UM).
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60 hours
|
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Tmax for solanidine, SSDA, m414, α-solanine and α-chaconine
Tidsram: 60 hours
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Time to maximum concentration (tmax) of solanidine, its CYP2D6-dependent metabolites SSDA and m414, and its parent molecules α-solanine and α-chaconine will be determined for each metabolizer status cohort (PM, LIM, EM, UM).
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60 hours
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Samarbetspartners och utredare
Sponsor
Studieavstämningsdatum
Studera stora datum
Studiestart (Beräknad)
Primärt slutförande (Beräknad)
Avslutad studie (Beräknad)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Faktisk)
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- IPHA-2026-12
Plan för individuella deltagardata (IPD)
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