ClinicalTrials.gg
CompletedNCT05287893Updated Apr 16, 2025Results posted

Pyronaridine in Healthy Adult Participants Infected With Blood Stage Malaria

A Phase 1 interventional study of Pyronaridine and P. falciparum IBSM infection in Malaria,Falciparum, Malaria and Malaria Recrudescence, sponsored by Medicines for Malaria Venture. Completed at 2 sites in Australia. Open to participants aged 18 Years to 55 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-04-16.

Sponsored by Medicines for Malaria Venture · Phase 1, Interventional, and Other

Phase
Phase 1
Study type
Interventional
Enrollment
10
Allocation
Randomized
Ages
18 Years to 55 Years
Sex
All
01

Study summary

This is an open-label, adaptive study that will utilise the P. falciparum induced blood stage malaria (IBSM) model to characterise the pharmacokinetic/pharmacodynamic (PK/PD) profile of pyronaridine. Up to 18 healthy, malaria naïve adult participants are planned to be enrolled into this study, in cohorts of up to six participants each. Following a screening period of up to 28 days, cohorts of up to 6 healthy participants will be enrolled. Each participant will be inoculated intravenously on Day 0 with P. falciparum infected erythrocytes. Participants will be followed up daily on Days 1 to 3, and will attend the clinical unit once on Days 4, 5, 6 and 7 for clinical evaluation and blood sampling. Participants will be admitted to the clinical trial unit on Day 8 for a single oral dose of pyronaridine.

Different doses of pyronaridine will be administered across and within cohorts. Participants will be randomised to a dose group on the day of dosing. The highest dose of pyronaridine administered will be no more than 720 mg; the lowest dose administered will be no less than 180 mg.

Each subsequent cohort will be composed of up to 3 dose groups. The Safety Data Review Team (SDRT) will review all available safety and tolerability data from the previous cohort/s prior to inoculation of the next cohort.

Participants will be confined in the clinical unit for at least 96 h (Days 8 - 12) to monitor the safety and tolerability of pyronaridine dosing. Upon discharge from the clinical unit participants will be monitored on an outpatient basis up to Day 50±2. Participants will receive compulsory antimalarial rescue treatment with Riamet® (artemether/lumefantrine) on Day 47±2 or earlier.

Read the detailed description

This is an open-label, adaptive study that will utilise the P. falciparum induced blood stage malaria (IBSM) model to characterise the pharmacokinetic/pharmacodynamic (PK/PD) profile of pyronaridine.

Up to 18 healthy, malaria naïve adult participants are planned to be enrolled into this study, in cohorts of up to six participants each. Following a screening period of up to 28 days, cohorts of up to 6 healthy participants will be enrolled. Each participant will be inoculated intravenously on Day 0 with approximately 2,800 viable P. falciparum infected erythrocytes. Participants will be followed up daily via phone call or text message on Days 1 to 3 post-inoculation to solicit any adverse events. Participants will attend the clinical unit once on Days 4, 5, 6 and 7 for clinical evaluation and blood sampling to monitor the progression of parasitaemia, using quantitative polymerase chain reaction (qPCR) targeting the gene encoding 18S rRNA (referred to hereafter as malaria 18S qPCR). Participants will have a nasopharyngeal aspirate (NPA) for SARS-CoV-2 on Day 6 am in the event that there is community transmission in South East Queensland of SARS-CoV-2. Participants will also have blood collected on Day 7 am to monitor haematology and biochemistry. Participants will be admitted to the clinical trial unit on Day 8 for dosing with the investigational medicinal product (IMP; pyronaridine) when parasitaemia for the majority of participants is expected to be above 5,000 parasites/mL. Pyronaridine will be administered as a single oral dose. Different doses of pyronaridine will be administered across and within cohorts in order to effectively characterise the PK/PD relationship. Each cohort will comprise up to three dose groups, with participants randomised to a dose group on the day of dosing. The highest dose of pyronaridine administered will be no more than 720 mg; the lowest dose administered will be no less than 180 mg. The proposed dosing regimen for the Cohort 1, assuming six participants are enrolled, is as below. If less than six participants are enrolled the Safety Data Review Team (SDRT) will meet between Day 0 and Day 8, to decide on the dose/s to be administered.

Dose group

1A (n=2) 360 mg

1B (n=2) 540 mg

1C (n=2) 720 mg

Each subsequent cohort will be composed of up to 3 dose groups. If more than one dose is tested in a given cohort, subjects will be randomised after inoculation day (Day 0) but prior to Day 8. The dose/s administered to Cohort 2 and Cohort 3 will be selected based on PK/PD and safety data from the preceding cohort/s. The SDRT will review all available safety and tolerability data and PK/PD analysis outcomes from the previous cohort/s prior to inoculation of the next cohort. The study will conclude when sufficient data have been obtained to define the PK/PD parameters for pyronaridine (the primary endpoint).

A maximum sample size of 18 participants administered pyronaridine is expected to be sufficient to achieve the primary endpoint.

Participants will be confined in the clinical unit for at least 96 h (Days 8 - 12) to monitor the safety and tolerability of pyronaridine dosing and to ensure adequate clinical response against P. falciparum. During confinement, regular safety assessments will be performed and blood will be collected to monitor parasite clearance and pyronaridine concentration. If participants are clinically well at the end of the confinement period, they will be discharged and monitored on an outpatient basis up to Day 50±2.

Participants will receive compulsory antimalarial rescue treatment with Riamet® (artemether/lumefantrine) on Day 47±2 or earlier.

02

Conditions studied

  • Malaria,Falciparum
  • Malaria
  • Malaria Recrudescence
  • Parasitemia
  • Protozoan Infections
  • Parasitic Disease

Keywords

  • Malaria
  • Malaria,Falciparum
  • Malaria Recrudescence
  • Parasitaemia
  • Pyronaridine
03

In context

Malaria, Falciparum

455 studies on the registry are indexed under Malaria, Falciparum; 37 are open to participants now.

This study's enrollment of 10 is below the median of 126 across 376 interventional studies indexed under Malaria, Falciparum.

Browse Malaria, Falciparum studies →

Lead sponsor

Medicines for Malaria Venture is the lead sponsor of 66 studies on the registry; 3 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 55 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

Demography

  1. Male or female (non-pregnant, non-lactating) aged 18 to 55 years inclusive who will be contactable and available for the duration of the trial and up to two weeks following the EOS visit.
  2. Total body weight greater than or equal to 50 kg, and a (BMI) within the range of 18 to 32 kg/m2 (inclusive). BMI is an estimate of body weight adjusted for height. It is calculated by dividing the weight in kilograms by the square of the height in metres.

    Health status

  3. Certified as healthy by a comprehensive clinical assessment (detailed medical history and full physical examination).
  4. Vital signs at screening (measured after 5 min in the supine position):

    • Systolic blood pressure (SBP) - 90-140 mmHg,
    • Diastolic blood pressure (DBP) - 40-90 mmHg,
    • Heart rate (HR) 40-100 bpm.
  5. At Screening and pre-inoculation with the malaria challenge agent: normal standard mean of triplicate 12-lead (ECG) parameters after 5 minutes resting in supine position in the following ranges:

    1. ≤450 msec (male participants); QTcF ≤470 msec (female participants);
    2. QRS 50-120 msec
    3. PR interval ≤ 210 msec for both males and females, and
    4. Normal ECG tracing unless the PI or delegate considers an ECG tracing abnormality to be not .
  6. Women of (WOCBP) who anticipate being sexually active with a male during the trial must agree to the use of a highly effective method of (see below) combined with a barrier contraceptive from the screening visit until 100 days after the last dose of pyronaridine (covering a full menstrual cycle of 30 days starting after 5 half-lives of last dose pyronaridine) and have a negative result on urine pregnancy test performed before inoculation with the malaria challenge agent.

Note:

a. Highly effective birth control methods include: combined (oestrogen and progestogen containing) oral/intravaginal/transdermal/implantable hormonal contraception associated with inhibition of ovulation, progestogen-only oral/injectable/implantable hormonal contraception associated with inhibition of ovulation, intrauterine device, intrauterine hormone-releasing system, bilateral tubal occlusion, vasectomised partner, or sexual abstinence or same sex relationship.

b. Female participants who are abstinent (from penile-vaginal intercourse) must agree to start a double method if they start a sexual relationship with a male during the study. Female participants must not be planning in vitro fertilisation within the required contraception period.

  1. Women of non-childbearing potential (WONCBP) are defined as:
  1. Natural (spontaneous) defined as being amenorrhoeic for at least 12 months without an alternative medical cause with a screening follicle stimulating hormone level (FSH) >25 IU/L (or at the local laboratory levels for post-menopause)
  2. Premenopausal with irreversible surgical sterilization by hysterectomy and/or bilateral oophorectomy or salpingectomy at least 6 months before screening (as determined by participant medical history) 8. Males who have, or may have, female sexual partners of child bearing potential during the course of the study must agree to use a double method of contraception including condom plus diaphragm, or condom plus intrauterine device, or condom plus stable oral/transdermal/injectable/implantable hormonal contraceptive by the female partner, from the time of through to 70 days (covering a spermatogenesis cycle) after pyronaridine administration. Abstinent males must agree to start a double method if they begin sexual relationship with a female during the study and up to 70 days after the last dose of pyronaridine. Males with female partners of child-bearing potential that are surgically sterile, or males who have undergone sterilisation and have had testing to confirm the success of the sterilisation, may also be included and will not be required to use above described methods of contraception.

    Regulations 9. Completion of the written informed consent process prior to undertaking any trial-related procedure.

    1. Must be willing and able to communicate and participate in the whole trial. 11. Agreement to adhere to Lifestyle Considerations (see Section 5.3) throughout trial duration 12. Agreement to provide current contact details (two telephone numbers including a mobile number and a responsible adult as an emergency contact) and a relevant email address.

Exclusion criteria

Exclusion Criteria:

  • Individual who lives alone, OR, does not satisfy the following criteria: Participants who live alone may be included on a case-by-case basis, following discussion with the Principal Investigator. Participants who live alone must identify and provide contact details of a support person who is aware of the participant's participation in the study and is available to provide assistance if required (for example with contacting the participant in the event that study staff are unable to, or with transporting the participant to and from the study site if required).

    1. Known to pyronaridine, artesunate or any of its derivatives, artemether, lumefantrine or other artemisinin derivatives, proguanil/atovaquone, primaquine, or 4-aminoquinolines.
    1. Haematology, biochemistry or urinalysis results at screening or at the eligibility visit that are outside of Sponsor-approved clinically acceptable laboratory ranges (appendix) or are considered by the PI or their delegate.
    1. Participation in any product trial within the 12 weeks preceding pyronaridine administration.
    1. Symptomatic postural hypotension at screening (confirmed on two consecutive readings), irrespective of the decrease in blood pressure, or asymptomatic postural hypotension defined as a decrease in systolic blood pressure ≥20 mmHg within 2-3 min when changing from supine to standing position.
    1. Any history of anaphylaxis or other severe allergic reactions including face, mouth, or throat swelling or any difficulty breathing, or other food or drug allergy that the Investigator considers may impact on participant safety. Participants with seasonal allergies/hay fever or allergy to animals or house dust mite that are untreated and asymptomatic at the time of dosing can be enrolled in the trial.
    1. History of convulsion (including drug or vaccine-induced episodes). A medical history of a single febrile convulsion during childhood (\< 5 years) is not an exclusion criterion.
    1. Presence of current or suspected serious chronic diseases such as cardiac or disease, diabetes, progressive neurological disease, severe malnutrition, hepatic or renal disease. Acute or progressive hepatic or renal disease, porphyria, psoriasis, rheumatoid arthritis, asthma (excluding childhood asthma, or mild asthma with preventative asthma medication required less than monthly), or epilepsy.
    1. History of of any organ system (other than localised basal cell carcinoma of the skin or in situ cervical cancer), treated or untreated, within five years of screening, regardless of whether there is evidence of local recurrence or .
    1. Individuals with history of schizophrenia, bipolar disorder psychoses, disorders requiring lithium, attempted or planned suicide, or any other severe (disabling) chronic psychiatric diagnosis including generalised anxiety disorder.
    1. Individuals who have been hospitalised within five years prior to enrolment for either a psychiatric illness or due to danger to self or others.

History of an episode of mild/moderate depression lasting more than 6 months that required pharmacological therapy and/or psychotherapy within the last 5 years; or any episode of major depression.

The Beck Depression Inventory-II (BDI-II) will be used as a validated tool for the assessment of depression at screening. In addition to the conditions listed above, participants with a score of 20 or more on the BDI-II and/or a response of 1, 2 or 3 for item 9 of this inventory (related to suicidal ideation) will not be eligible for participation. These participants will be referred to a general practitioner or medical specialist as appropriate. Participants with a BDI-II score of 17 to 19 may be enrolled at the discretion of an Investigator if they do not have a history of the psychiatric conditions mentioned in this criterion and their mental state is not considered to pose additional risk to the health of the participant or to the execution of the trial and interpretation of the data gathered.

  1. History of recurrent headache (e.g. tension-type, cluster, or migraine) with a frequency of ≥2 episodes per month on average and severe enough to require medical therapy, during the 2 years preceding screening.
  1. Presence of clinically significant infectious disease or fever (e.g., sublingual temperature ≥38.5°C) within the five days prior to inoculation.
  1. Blood product donation to any blood bank during the 8 weeks (whole blood) or 4 weeks (plasma and ) prior to admission in the clinical unit on Day 8.
  1. History or presence of alcohol abuse (alcohol consumption more than 40 g/4 units/4 standard drinks per day), or drug habituation, or any prior intravenous usage of an illicit substance.
  1. Any individual who currently (within 14 days prior to inoculation) smokes >5 cigarettes/day.
  1. Breastfeeding or lactating; positive serum pregnancy test at screening, positive urine pregnancy test upon admission or at other time points as specified by schedule of activities tables.
  1. Any COVID-19 vaccine within 14 days of inoculation, any other vaccination within 28 days of IMP intake, and any vaccination (including COVID-19 initial or second dose) planned up to the final follow-up visit.
  1. Any , anti-inflammatory drugs (excluding commonly used over-the-counter anti-inflammatory drugs such as ibuprofen, acetylsalicylic acid, diclofenac), immunomodulators or anticoagulants within the past three months. Any individual currently receiving or having previously received therapy (including systemic steroids, adrenocorticotrophic hormone or inhaled steroids) at a dose or duration potentially associated with hypothalamic-pituitary-adrenal axis suppression within the past year.
  1. Use of prescription drugs (excluding ) or non-prescription drugs or herbal supplements (such as St John's Wort), within 14 days or five half-lives (whichever is longer) prior to inoculation. Limited use of other non-prescription medications or dietary supplements, not believed to affect participant safety or the overall results of the trial, may be permitted on a case-by-case basis following approval by the Sponsor in consultation with the PI. Participants are requested to refrain from taking non-approved concomitant medications from recruitment until the conclusion of the trial.
  1. Cardiac/ risk: Family history of sudden death or of congenital prolongation of the QTc interval or known congenital prolongation of the QTc interval or any clinical condition known to prolong the QTc interval.

History of symptomatic cardiac arrhythmias or with clinically relevant bradycardia.

  1. Any history of malaria or participation in a previous malaria challenge trial or malaria vaccine trial.
  1. Must not have had malaria exposure that is considered by the PI or their delegate to be significant. This includes but is not limited to: history of having travelled to or lived (>2 weeks) in a malaria-endemic region during the past 12 months or planned travel to a malaria-endemic region during the course of the trial; history of having lived for >1 year in a malaria-endemic region in the past 10 years; history of having ever lived in a malaria-endemic region for more than 10 years inclusive. For endemic regions see https://malariaatlas.org/explorer/#/, Bali is not considered a malaria-endemic region.
  1. Has evidence of increased cardiovascular disease risk (defined as >10%, 5-year risk for those greater than 35 years of age, as determined by the Australian Absolute Cardiovascular Disease Risk Calculator [http://www.cvdcheck.org.au/]). Risk factors include sex, age, systolic blood pressure (mm/Hg), smoking status, total and HDL cholesterol (mmol/L), and reported diabetes status.
  1. History of splenectomy. 27. Individual unwilling to defer blood donations to the Blood Service for at least twelve months after the EOS visit.
  1. Individual who has ever received a blood transfusion. 29. Any recent (\<6 weeks) therapy with an antibiotic or drug with potential antimalarial activity (e.g. chloroquine, piperaquine phosphate, benzodiazepine, flunarizine, fluoxetine, tetracycline, azithromycin, clindamycin, doxycycline etc.).

General conditions 30. Any individual who, in the judgement of an Investigator, is likely to be non-compliant during the trial, or is unable to cooperate because of a language problem or poor mental development.

  1. Any individual in the exclusion period of a previous trial according to applicable regulations.
  1. Any individual who is an Investigator, research assistant, pharmacist, trial coordinator, or other staff thereof, directly involved in conducting the trial.
  1. Any individual without good peripheral venous access. Biological status 34. Positive result on any of the following tests: surface antigen (HBs Ag), anti-hepatitis B core antibodies (anti-HBc Ab), anti- virus (anti-HCV) antibodies, anti- 1 and 2 antibodies (anti-HIV1 and anti-HIV2 Ab).
  1. Positive urine drug test. Any drug listed in the urine drug screen unless there is an explanation acceptable to an Investigator (e.g., the participant has stated in advance that they consumed a prescription or over-the-counter product that contained the detected drug) and the participant has a negative urine drug screen on retest by the pathology laboratory.
  1. Severe G6PD deficiency. 37. Positive alcohol breath test. 38. Positive for SARS-CoV-2 by PCR. NPA testing is to occur between Day -3 to Day -1 but only in the event that there is community transmission in South East Queensland (see section 8.3.7) 39. Positive for red cell antibodies
Terms in these criteria, in plain language(19)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

BMI (body mass index)

Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.

What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.

ECG (electrocardiogram)

A recording of the heart’s electrical activity, taken with stickers on the chest, arms and legs. It takes a few minutes and does not hurt.

QT and QTc

On an ECG, the QT interval is the time the heart’s lower chambers take to activate electrically and recover in each beat. QTc is that time adjusted for heart rate (QTcF by Fridericia’s formula, QTcB by Bazett’s). Some medicines lengthen it, and a long QTc can raise the risk of a dangerous heart rhythm.

The study may name a correction formula and a limit in milliseconds, often around 450–480.

Clinically significant

Judged by the study doctor to matter for your health or for the study. It is a doctor’s decision, so ask the study team if you are unsure whether something counts.

Childbearing potential

Able to become pregnant: from the first period until menopause, unless permanently unable to through surgery (removal of the womb, or of both ovaries or both fallopian tubes).

Criteria for people of childbearing potential usually ask for a negative pregnancy test and for contraception during the study and for a time after it.

Contraception

Ways of preventing pregnancy. “Highly effective” methods fail less than 1% of the time a year when used correctly — for example an IUD or an implant.

Criteria usually say which methods count and how long to keep using them after the last dose, sometimes for male participants too. Some studies accept a partner’s vasectomy if it was confirmed successful and that person is the participant’s only sexual partner.

Postmenopausal

Periods have stopped for good: usually no period for 12 months in a row without another medical reason, sometimes confirmed by a blood test (FSH).

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

Hypersensitivity

An allergy, or another reaction of the immune system, to a substance. “Hypersensitivity to the study drug” means a known allergic reaction to it — not every side effect a medicine can have.

Investigational drug or device

A drug or device being studied in a clinical trial.

It may be new, or already approved and being studied for another use, dose or form. Criteria often leave out people who took part in another study of one within a recent period, commonly 30 days or five half-lives.

Autoimmune disease

A condition in which the immune system attacks the body’s own tissues, such as rheumatoid arthritis, lupus, psoriasis, type 1 diabetes or inflammatory bowel disease.

Immunotherapy studies often leave out active autoimmune disease, and some name exceptions, such as thyroid disease on replacement hormone. Check the exceptions this study lists.

Cancer (malignancy)

Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.

Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.

Metastases

Cancer that has spread from where it began to other parts of the body. “Metastatic” cancer is cancer that has spread this way.

Platelets

Blood cells that help blood clot. Too few raises the risk of bleeding and bruising. A usual adult range is about 150–400 × 10⁹/L (150,000–400,000 per µL); each lab has its own reference range.

Corticosteroids (steroids)

Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.

Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.

Immunosuppression

A weakened immune system. It can come from an illness, such as HIV or some blood cancers, or from medicines that turn the immune system down, for example after an organ transplant or for an autoimmune disease; steroids at higher doses count.

Read whether the line is about a condition or about medicines, and which medicines and doses it means.

Hepatitis B tests

Hepatitis B is a virus that infects the liver. These are separate tests: HBsAg positive usually means a current infection (a recent vaccination can briefly cause it too); total anti-HBc (HBcAb) positive means an infection now or in the past; HBV DNA measures how much virus is in the blood.

Some studies accept a past infection if HBV DNA is undetectable, sometimes with antiviral medicine during the study. Check what this study allows.

Hepatitis C tests

Hepatitis C is a virus that infects the liver. An HCV antibody test can stay positive after an infection has cleared (and is occasionally positive without one); an HCV RNA test shows whether the virus is there now.

After treatment, hepatitis C counts as cured when HCV RNA is still undetectable 12 weeks or more after the treatment ended. Studies often accept people cured this way.

HIV

The human immunodeficiency virus, which weakens the immune system.

Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.

05

Study design

Phase
Phase 1
Primary purpose
Other
Allocation
Randomized
Intervention model
Sequential assignment
Masking
None (open label)
Enrollment
10 participants (actual)

Study arms

  • Experimental
    Pyronaridine 360 mg

    Up to 18 healthy, malaria naïve adult participants are planned to be enrolled into this study, in cohorts of up to six participants each. on Day 0 participants will be inoculated intravenously with approximately 2,800 viable P. falciparum-infected erythrocytes. Day 8 participants will be dosed with pyronaridine when parasitaemia for the majority of participants is expected to be above 5,000 parasites/mL. Different doses of pyronaridine will be administered across and within cohorts in order to effectively characterise the PK/PD relationship. Regular safety assessments will be performed and blood will be collected to monitor parasite clearance and pyronaridine concentration. Participants will receive compulsory antimalarial rescue treatment with Riamet® (artemether/lumefantrine) on Day 47±2, or earlier.

    Drug: Pyronaridine · Biological: P. falciparum IBSM infection

  • Experimental
    Pyronaridine 540 mg

    Up to 18 healthy, malaria naïve adult participants are planned to be enrolled into this study, in cohorts of up to six participants each. on Day 0 participants will be inoculated intravenously with approximately 2,800 viable P. falciparum-infected erythrocytes. Day 8 participants will be dosed with pyronaridine when parasitaemia for the majority of participants is expected to be above 5,000 parasites/mL. Different doses of pyronaridine will be administered across and within cohorts in order to effectively characterise the PK/PD relationship. Regular safety assessments will be performed and blood will be collected to monitor parasite clearance and pyronaridine concentration. Participants will receive compulsory antimalarial rescue treatment with Riamet® (artemether/lumefantrine) on Day 47±2, or earlier.

    Drug: Pyronaridine · Biological: P. falciparum IBSM infection

  • Experimental
    Pyronaridine 720 mg

    Up to 18 healthy, malaria naïve adult participants are planned to be enrolled into this study, in cohorts of up to six participants each. on Day 0 participants will be inoculated intravenously with approximately 2,800 viable P. falciparum-infected erythrocytes. Day 8 participants will be dosed with pyronaridine when parasitaemia for the majority of participants is expected to be above 5,000 parasites/mL. Different doses of pyronaridine will be administered across and within cohorts in order to effectively characterise the PK/PD relationship. Regular safety assessments will be performed and blood will be collected to monitor parasite clearance and pyronaridine concentration. Participants will receive compulsory antimalarial rescue treatment with Riamet® (artemether/lumefantrine) on Day 47±2, or earlier.

    Drug: Pyronaridine · Biological: P. falciparum IBSM infection

  • Other
    Not treated

    This inoculated participant was treated with rescue medication instead of pyronaridine due to testing positive for SARS-CoV-2 (COVID-19). Ten (10) participants were inoculated with P. falciparum and were included in the Full Analysis Set (FAS). Nine (9) inoculated participants were subsequently administered pyronaridine, and were included in the IMP Set, PK Analysis Set, PD Analysis Set, and the PK/PD Analysis Set. Some of the 18S qPCR data for the inoculated participant who was not administered pyronaridine was used in the PD model for PK/PD analyses.

    Biological: P. falciparum IBSM infection

Interventions

  • Single dose

  • BiologicalP. falciparum IBSM infection

    Induced Blood Stage Malaria

06

What researchers measure

Primary outcomes

  1. Emax

    Maximum drug killing rate, calculated using the combined data from all doses/arms/groups in both period 1 and 2, as prespecified in section 10 of the Statistical Analysis Plan. The PKPD relationship was identified using SysFit as an Emax model with the parameters estimated from the parasitaemia data.

    Time frame: Day 8 to Day 50+/-2

  2. EC50

    Half Maximal Effective Concentration Calculated using the combined data from all doses/arms/groups in both period 1 and 2, as prespecified in section 10 of the Statistical Analysis Plan. The PKPD relationship was identified using SysFit as an Emax model with the parameters estimated from the parasitaemia data.

    Time frame: Day 8 to Day 50+/-2

  3. Hill Coefficient

    Hill coefficient is the slope of the drug concentration-response curve (i.e. response in this study is the parasite killing). Calculated using the combined data from all doses/arms/groups in both period 1 and 2, as prespecified in section 10 of the Statistical Analysis Plan. The PKPD relationship was identified using SysFit as an Emax model with the parameters estimated from the parasitaemia data. The "Emax-model" assumes a direct effect of concentrations on parasite killing/clearance, such as: Kill = Emax x (Cc\^Hill /(Cc\^Hill + EC50\^Hill)) where Cc is the concentration in the central compartment, Emax is the maximum effect of the drug, EC50 is the concentration that results in 50% of the maximum effect, and Hill is the Hill coefficient.

    Time frame: Day 8 to Day 50+/-2

  4. Minimum Inhibitory Concentration (MIC)

    MIC is defined as the concentration when drug killing equals the parasite growth, i.e., the time at which the minimum parasite concentration is observed. Calculated using the combined data from all doses/arms/groups in both period 1 and 2, as prespecified in section 10 of the Statistical Analysis Plan.

    Time frame: Day 8 to Day 50+/-2

  5. Minimal Parasiticidal Concentration (MPC90)

    MPC90 is defined as the concentration at which the clearance effect is at 90% of the maximum. Calculated using the combined data from all doses/arms/groups in both period 1 and 2, as prespecified in section 10 of the Statistical Analysis Plan.

    Time frame: Day 8 to Day 50+/-2

  6. Parasite Reduction Ratio in 48 h (log10PRR48)

    PRR48 is defined as the parasite reduction ratio achieved within 48 hours, usually given as the reduction of values on log10 transformed scale. PRR48 provides an efficacy estimate of anti-malarial treatment and is the ratio of the parasite density over a 48 hour time-period. PRR48 is estimated using the slope of the optimal fit of the log-linear relationship of the parasitemia decay. Optimal fit is derived using the geometric mean parasitemia data (i.e. 18S qPCR measuring all blood stage malaria parasites). Optimal fit of log-linear parasitemia by time relationship is determined using left and right censoring to systematically remove potential lag phase and tail phase of parasitemia decay. The PRR48 was calculated per subject in MMV_PYR using daily PCR data; and if the model fit was adequate for the subject (defined as overall model p-value\<0.001), the slope and corresponding standard error (SE) from the log-linear regression was used to calculate the overall dose-specific PRR48

    Time frame: Day 8 to Day 50+/-2

07

Results

Posted Apr 16, 2025

Participant flow

Initial Randomization and PKPD Modelling
Participant flow — Initial Randomization and PKPD Modelling
MilestoneCohort 1: Pyronaridine 360 mgCohort 1: Pyronaridine 540 mgCohort 1: Pyronaridine 720 mgUntreatedCohort 2: Pyronaridine 360 mgCohort 2: Pyronaridine 540 mg
Started221100
Completed221100
Not completed000000
Cohort 2 Dosing and Modelling
Participant flow — Cohort 2 Dosing and Modelling
MilestoneCohort 1: Pyronaridine 360 mgCohort 1: Pyronaridine 540 mgCohort 1: Pyronaridine 720 mgUntreatedCohort 2: Pyronaridine 360 mgCohort 2: Pyronaridine 540 mg
Started000022
Completed000020
Not completed000002

Outcome measures

PrimaryEmax

Maximum drug killing rate, calculated using the combined data from all doses/arms/groups in both period 1 and 2, as prespecified in section 10 of the Statistical Analysis Plan. The PKPD relationship was identified using SysFit as an Emax model with the parameters estimated from the parasitaemia data.

Time frame:
Day 8 to Day 50+/-2
Reported as:
Mean · Maximum clearance rate (1/hour)
Emax
Maximum clearance rate (1/hour)IBSM Challenge and Pyronaridine PK/PD Population Profile
Emax0.201 ± 3.87
PrimaryEC50

Half Maximal Effective Concentration Calculated using the combined data from all doses/arms/groups in both period 1 and 2, as prespecified in section 10 of the Statistical Analysis Plan. The PKPD relationship was identified using SysFit as an Emax model with the parameters estimated from the parasitaemia data.

Time frame:
Day 8 to Day 50+/-2
Reported as:
Mean · μg/mL
EC50
μg/mLIBSM Challenge and Pyronaridine PK/PD Population Profile
EC500.00575 ± 11.3
PrimaryHill Coefficient

Hill coefficient is the slope of the drug concentration-response curve (i.e. response in this study is the parasite killing). Calculated using the combined data from all doses/arms/groups in both period 1 and 2, as prespecified in section 10 of the Statistical Analysis Plan. The PKPD relationship was identified using SysFit as an Emax model with the parameters estimated from the parasitaemia data. The "Emax-model" assumes a direct effect of concentrations on parasite killing/clearance, such as: Kill = Emax x (Cc\^Hill /(Cc\^Hill + EC50\^Hill)) where Cc is the concentration in the central compartment, Emax is the maximum effect of the drug, EC50 is the concentration that results in 50% of the maximum effect, and Hill is the Hill coefficient.

Time frame:
Day 8 to Day 50+/-2
Reported as:
Mean · Hill Coefficient
Hill Coefficient
Hill CoefficientIBSM Challenge and Pyronaridine PK/PD Population Profile
Hill Coefficient6.62 ± 2.42
PrimaryMinimum Inhibitory Concentration (MIC)

MIC is defined as the concentration when drug killing equals the parasite growth, i.e., the time at which the minimum parasite concentration is observed. Calculated using the combined data from all doses/arms/groups in both period 1 and 2, as prespecified in section 10 of the Statistical Analysis Plan.

Time frame:
Day 8 to Day 50+/-2
Reported as:
Median · ng/mL
Minimum Inhibitory Concentration (MIC)
ng/mLIBSM Challenge and Pyronaridine PK/PD Population Profile
Minimum Inhibitory Concentration (MIC)5.5 (4.3 to 6.9)
PrimaryMinimal Parasiticidal Concentration (MPC90)

MPC90 is defined as the concentration at which the clearance effect is at 90% of the maximum. Calculated using the combined data from all doses/arms/groups in both period 1 and 2, as prespecified in section 10 of the Statistical Analysis Plan.

Time frame:
Day 8 to Day 50+/-2
Reported as:
Median · ng/mL
Minimal Parasiticidal Concentration (MPC90)
ng/mLIBSM Challenge and Pyronaridine PK/PD Population Profile
Minimal Parasiticidal Concentration (MPC90)8 (6.4 to 10)
PrimaryParasite Reduction Ratio in 48 h (log10PRR48)

PRR48 is defined as the parasite reduction ratio achieved within 48 hours, usually given as the reduction of values on log10 transformed scale. PRR48 provides an efficacy estimate of anti-malarial treatment and is the ratio of the parasite density over a 48 hour time-period. PRR48 is estimated using the slope of the optimal fit of the log-linear relationship of the parasitemia decay. Optimal fit is derived using the geometric mean parasitemia data (i.e. 18S qPCR measuring all blood stage malaria parasites). Optimal fit of log-linear parasitemia by time relationship is determined using left and right censoring to systematically remove potential lag phase and tail phase of parasitemia decay. The PRR48 was calculated per subject in MMV_PYR using daily PCR data; and if the model fit was adequate for the subject (defined as overall model p-value\<0.001), the slope and corresponding standard error (SE) from the log-linear regression was used to calculate the overall dose-specific PRR48

Time frame:
Day 8 to Day 50+/-2
Reported as:
Geometric mean · log[(parasites/mL)/hour]
Parasite Reduction Ratio in 48 h (log10PRR48)
log[(parasites/mL)/hour]Pyronaridine 360 mgPyronaridine 540 mgPyronaridine 720 mg
Parasite Reduction Ratio in 48 h (log10PRR48)2.58 (2.43 to 2.74)2.53 (2.37 to 2.68)2.85 (2.65 to 3.06)

Adverse events

Collected over The period of observation for collection of AEs extends from the time of inoculation with the malaria challenge agent (Day 0) to EOS (Day 50+/-2). A total maximum of 53 days.. Non-serious events are listed at a 0% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Pyronaridine 360 mg0/4 (0%)0/4 (0%)4/4 (100%)
Pyronaridine 540 mg0/4 (0%)0/4 (0%)4/4 (100%)
Pyronaridine 720 mg0/1 (0%)0/1 (0%)1/1 (100%)
Most frequent other events
Showing 10 of 36
Most frequent other events
EventPyronaridine 360 mgPyronaridine 540 mgPyronaridine 720 mg
Abdominal pain upperGastrointestinal disorders0/40/41/1
NauseaGastrointestinal disorders2/41/41/1
ChillsGeneral disorders1/41/41/1
FatigueGeneral disorders2/43/41/1
PyrexiaGeneral disorders1/43/41/1
Covid-19Infections and infestations0/41/41/1
Decreased appetiteMetabolism and nutrition disorders1/41/41/1
HeadacheNervous system disorders3/42/41/1
DyspnoeaRespiratory, thoracic and mediastinal disorders0/40/41/1
Nasal congestionRespiratory, thoracic and mediastinal disorders1/41/41/1

Baseline characteristics

10 participants received inoculum and were included in the Full Analysis Set. 9 inoculated participants received 360mg (n=4), 560mg (n=4), or 720mg (n=1) pyronaridine, and included in the IMP Set, PK Analysis Set, PD Analysis Set, and the PK/PD Analysis Set. Some of the 18S qPCR data for the inoculated participant who was not administered pyronaridine was used in the PD model for PK/PD analyses. Analysis and results were grouped per dose/arm, not per cohort.

Age, Continuous
Age, Continuous(years)Pyronaridine 360 mgPyronaridine 540 mgPyronaridine 720 mgUntreatedTotal
Mean30.08 ± 7.4636.0 ± 14.8119.0 ± NA42.0 ± NA32.8 ± 11.34
Sex: Female, Male
Sex: Female, Male(Participants)Pyronaridine 360 mgPyronaridine 540 mgPyronaridine 720 mgUntreatedTotal
Female01113
Male43007
Race/Ethnicity, Customized
Race/Ethnicity, Customized(Participants)Pyronaridine 360 mgPyronaridine 540 mgPyronaridine 720 mgUntreatedTotal
Race — White24118
Race — Asian10001
Race — Other10001
Region of Enrollment
Region of Enrollment(Participants)Pyronaridine 360 mgPyronaridine 540 mgPyronaridine 720 mgUntreatedTotal
Australia441110
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Study locations

2 sites
  • South Bank
    Brisbane, Queensland 4101, Australia
  • USC Clinical Trials, Morayfield
    Brisbane, Queensland 4506, Australia
09

References and documents

Study documents

PDFs hosted by the registry, ClinicalTrials.gov.

Individual participant data

Plan to share: No

10

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Apr 2022 to primary completion in Sep 2022, 5 months.

Results were first posted in Apr 2025, 2 years 6 months after primary completion.

Of 29 non-industry phase 1 interventional studies under Malaria, Falciparum, half reached primary completion within 12 months of starting (the median), counting those still running; a quarter within 5 and three quarters within 24. This study's 5 months is below that.

Counting every sponsor, half of 49 studies reached it within 13 months; a quarter within 7 and three quarters within 18.

How these figures are worked out, and which studies are left out of them.

Registered
Mar 10, 2022
First posted
Mar 18, 2022
StartActual
Apr 4, 2022
Primary completionActual
Sep 26, 2022
CompletionActual
Sep 26, 2022
Results first posted
Apr 16, 2025
Last update
Apr 16, 2025
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Apr 16, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT05287893
Lead sponsor
Medicines for Malaria Venture
Collaborators
QIMR Berghofer Medical Research Institute, Southern Star Research, Swiss BioQuant, Children's Health Queensland Hospital and Health Service
Responsible party
Sponsor
First posted
Mar 18, 2022
Start date
Apr 4, 2022
Primary completion
Sep 26, 2022
Completion
Sep 26, 2022
Results posted
Apr 16, 2025
Last update
Apr 16, 2025

Study contacts

Jörg Möhrle, PhD
study director · Medicines for Malaria Venture

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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Studies of the drug tested here: Pyronaridine

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