Primary Immunodeficiency DiseasePhase 3BoyaIVIGNCT06150833
IVIG Boya: Safety, Efficacy, and Pharmacokinetics
A Phase 3 study testing Boya IVIG in people with Primary Immunodeficiency Disease, run by Azidus Brasil.
Trial summary
The goal of this phase 3, open-label, single-group clinical trial is to assess the efficacy of Boya IVIG in maintaining the mean number of serious bacterial infections to less than one per year in participants with primary immunodeficiency (PYD) due to common variable immunodeficiency (CVID), as defined by the… Read more about this study
- Who is it for?
- Ages 2 to 60 years
- Conditions the study is for
- Primary Immunodeficiency Disease
- What is being tested?
- Boya IVIG
- Type of treatment
- Injection or infusion
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 50 participants
- Where
- No sites listed yet
- Study dates
- Sep 2026to Sep 2028
- Phase
- Phase 3
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 2 to 60 years
- All sexes
- No healthy volunteers
- Child, Adult
Who may be able to join
- Men or women; age between 02 and 60 years; written informed consent/assent.
- Diagnosis of primary immunodeficiency disease (PID) with decreased antibody production due to common variable immunodeficiency (CVID) or X-linked agammaglobulinemia (XLA).
- Treatment-naïve patients and those receiving intravenous immunoglobulin replacement therapy at 21- to 28-day intervals, with doses ranging from 300 to 800 mg/kg per infusion.
- Negative pregnancy test in females of childbearing potential; willingness to use effective contraceptive methods throughout the study.
- Subjects currently receiving any subcutaneous or intramuscular immunoglobulin may be enrolled by switching to IVIG therapy at the investigator's discretion, considering the potential benefit to the participant.
- Exclusion Criteria Patients who meet any of the following criteria will be disqualified from participating.
Show all 41Show fewer
- Known intolerance or hypersensitivity to immunoglobulins or components of the study drug.
- Any contraindications to the use of immunoglobulins.
- Patients with a BMI < 18.5 or > 40 kg/m2.
- Secondary immunodeficiency or clinical conditions that potentially cause secondary immunodeficiency, such as chronic lymphocytic leukemia, lymphoma, multiple myeloma, enteropathies, or nephropathies with protein loss and hypoalbuminemia.
- Clinically significant changes in safety assessments, defined as:
- Blood count
- Hb < 10,5 g/dL
- Leukocytes < 3,000 cells/mm3 or > 11,000 cells/mm3
- Absolute neutrophil count < 1,000 cells/mm3
- Coagulation:
- o PT and aPTT> 2,5 x ULN.
- Biochemistry:
- glycated hemoglobin > 6.5%
- total bilirubin and fractions, alkaline phosphatase, ALT, AST, GGT > 2.5 x ULN
- creatinine above 3mg/dL or creatinine clearance <30mL/min
- Urine I:
- Clinically significant leukocyturia at the discretion of the investigator.
- History of serious bacterial infections within three months before screening, presence of an active infection at the time of inclusion, and failure to fully resolve any non-serious infection at least two weeks before screening.
- Any febrile illness in the 14 days before inclusion.
- Any active or resolved cancer in the last 12 months before screening.
- Receiving any blood products (except intravenous immunoglobulins) during the last 3 months before screening.
- History of thrombotic events (including myocardial infarction, cerebral vascular accident [including stroke], pulmonary embolism, and deep vein thrombosis) within the last 6 months before enrollment or the presence of significant risk factors for thrombosis events.
- Previous use of live attenuated virus vaccines within 3 months before enrollment.
- Selective immunoglobulin A (IgA) deficiency or the presence of known antibodies against IgA.
- Pregnancy, unreliable contraceptive methods, or lactation period (women only)
- Known alcohol or drug abuse.
- Patients with mental disorders that, in the investigator's opinion, may affect adherence to the protocol.
- Other primary immunodeficiencies (PIDs) besides CVID or XLA.
- Inability to comply with protocol activities.
- Patients who are infected with HIV, HBV, HCV, or syphilis.
- Any surgery scheduled to occur during the trial period.
- Patients with cystic fibrosis
- Patients with poorly controlled epilepsy, migraine, or hypertension (SBP ≥ 160 and/or DBP ≥ 100) managed with medication.
- Subjects who have finished participation in a clinical trial with another experimental IVIG, less than one year before enrollment, may be included if they have a potential benefit as per CNS Res. 251/1997.
- Any other medical condition that, in the investigator's opinion, may increase the risk of participation in this study.
Who cannot join
None listed.
Trial locations and contacts
No sites are listed yet. Contact the study team or a site near you to ask about taking part.
About this study
Official title: Evaluating the Safety, Effectiveness, and Pharmacokinetics of Boya Intravenous Immune Globulin in Patients With Primary Immune Deficiency.
The goal of this phase 3, open-label, single-group clinical trial is to assess the efficacy of Boya IVIG in maintaining the mean number of serious bacterial infections to less than one per year in participants with primary immunodeficiency (PYD) due to common variable immunodeficiency (CVID), as defined by the European Immunodeficiency Society (ESCID) / Pan American Immunodeficiency Group (PAGID), or X-linked agammaglobulinemia (XLA), as defined by molecular genetic testing (ESCID/PAGID).
The safety and pharmacokinetics (PK) of the investigational product will also be evaluated.
Read more
Participants must:
- Visit the research center every 21 or 28 days to receive the experimental product infusion and undergo a medical examination.
- During weekly telephone calls, report, if applicable, adverse events and hospitalizations; the number of school or workdays missed due to infections; the length of hospital stay; and the use of antibiotics for therapeutic purposes.
Read the detailed description
Fifty male or female participants aged 2 to 60 years, either treatment-naive or already receiving intravenous immunoglobulin replacement therapy, will be enrolled, including at least 20 participants aged 2 to 17 years. The study will also examine the pharmacokinetic (PK) profile in adult participants.
After obtaining signed informed consent or assent, screening will include reviewing immunodeficiency history in medical records, performing safety examinations, and assessing eligibility against inclusion and exclusion criteria.
Subjects who pass screening will begin a 6-visit run-in period. For participants already receiving treatment, the interval between intravenous injections should remain as prescribed before enrollment unless modified during the run-in period. During this period, participants will receive the study IVIG. For treatment-naïve participants, the dose and administration interval during the run-in will be determined by the Investigator.
After the run-in, the one-year trial will begin at V0. Study visits will be scheduled every 21 or 28 days, based on the participant's prescribed treatment plan. Each visit will have a ±3-day window around the scheduled date. At each visit, blood samples will be collected immediately before each IVIG dose to measure IgG trough levels. If a visit occurs earlier or later than the scheduled date, whether within or outside the allowed window, the timing of the next visit will be based on the actual date of the previous visit to maintain consistent planned inter-visit intervals throughout the study.
The V0 assessment will begin when participants have IgG concentrations ≥5 g/L on two consecutive infusions under the same dosing conditions. Therefore, the run-in period may include only two visits. If, among the six visits, the trough IgG concentration does not reach 5 g/L on two consecutive visits, the participant will be considered to have failed screening but may be rescreened.
To characterize the pharmacokinetic (PK) profile of the investigational product, at least 20 adult participants will undergo additional blood sampling between two consecutive study visits to measure total IgG concentrations and antigen-specific antibody levels, including anti-pneumococcal capsular polysaccharide, anti-Haemophilus influenzae, and anti-measles antibodies.
PK sampling should preferably be performed at Visit 4 (V4), provided that a stable dosing regimen has been maintained. Participants receiving IVIG on a 21-day schedule should collect seven samples at 30 minutes, 2 hours, 24 hours, 72 hours, 7 days, 14 days, and 21 days post-infusion. Participants receiving IVIG on a 28-day schedule should collect eight additional samples at 30 minutes, 2 hours, 24 hours, 72 hours, 14 days, 21 days, and 28 days post-infusion.
The PK profile should be evaluated only after at least four consecutive dosing intervals with no changes in posology, meaning both the dose and dosing interval remain unchanged, preferably at Visit 4 (V4). If any dose or interval adjustments occur between V0 and V4, PK profile sampling should be delayed until the next visit, after dosage stability is confirmed.
Participants will be contacted weekly between infusions to collect data on adverse events, concomitant medications, duration of infection treatment, and time lost from work or school due to infections during the period.
Additionally, subjects will have continued access to the investigator's team to report adverse events and to receive advice on next steps or additional medical evaluations, if necessary.
Medical evaluation, vital signs, and oximetry, adverse events, and concomitant medication will be assessed at all visits.
Safety laboratory tests (including direct Coombs and pregnancy tests) will be performed at every 4th or 5th visit.
- Conditions
- Primary Immunodeficiency Disease
- Being tested
- Boya IVIG
- Keywords
- IVIG, primary immunodeficiency disease, PID, common variable immunodeficiency, CVID, X-linked agammaglobulinemia, XLA
- Medical subject headings
- Primary Immunodeficiency Diseases, Common Variable Immunodeficiency, Bruton type agammaglobulinemia
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Boya IVIGBiological
Also called IVIG, BOYA
Intervention:
Biological: Boya IVIG Boya IVIG is a 5% human immunoglobulin for intravenous administration
| Study group | Role | What they receive |
|---|---|---|
| Boya IVIG | Experimental | All participants will receive Boya IVIG:
Dose: 200 to 800 mg/kg Schedule of administration: 21- or 28-day interval Time frame: 54 weeks (21-day interval) or 56 weeks (28-day interval) Receives: Biological: Boya IVIG |
What is being measured
The primary outcome is the main question the study is designed to answer.
Primary Efficacy Objective
Average incidence of serious bacterial infections per participant between V0 and Vfinal.
Measured: 54 weeks (21-day interval schedule) or 56 weeks (28-day interval schedule)
Secondary outcomes (4)
Assessment of the rate of non-serious infections within one year
The incidence of all acute infections except the serious acute bacterial infections within the 1-year follow-up (simple descriptive statistics).
Measured: Average incidence of non-serious infections per patient between Visit 0 and Final Visit (through study completion, an average of 1 year), as documented as treatment emergent adverse events (TEAEs).
Missing time from school/work
Assessment of time lost at school/work due to infections per year
Measured: Average number of days off from school/work per patient/year, as collected in weekly telephone contacts.
Length of hospitalization
Assessment of the length of hospital stay per year.
Measured: Number of days of hospitalization due to infections per participant/year between V0 and Vfinal, as documented as Adverse Events.
Use of antibiotics
Assess the use of antibiotics for therapeutic purposes.
Measured: Tabulation of all antibiotics used, separating those indicated for prophylactic and therapeutic purposes
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted29 Nov 2023
- Study startSep 2026 (estimated)
- Primary completionSep 2028 (estimated)
- Study completionSep 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (4)Papers the sponsor has linked to this study.
- Other trials for Primary Immunodeficiency DiseaseStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 3
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Model description
- Patients with primary immunodeficiency will start therapy or switch to Boya IVIG and optimize the posology in a run-in period of 2 to 6 administrations. In the one-year test period, the patients will receive the test IVIG at 21- or 28-day intervals and be followed. IgG trough levels will be collected from all participants, at all visits. The pharmacokinetic profile will be measured after 5 infusions with stable dose in 20 adult participants, collecting additional blood samples.
- Masking
- None (open label)
- Enrolment
- 50 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Azidus Brasil
- Sponsor type
- Industry (pharma, biotech, devices)
- Collaborators
- Boya Bio Pharmaceutical Group Co Ltd
- Responsible party
- Sponsor
- Investigators
- Luciana Ferrara, Study director, Azidus Brasil
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06150833
- Sponsor's protocol ID
- BoyaIVIG
- Acronym
- BoyaIVIG
- Status last verified
- May 2026
- First submitted
- 21 Nov 2023
- Last updated
- 3 Jun 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: It is believed that after the data analysis and presentation to the National Commission on Research Ethics, all data of the study will become public.
Publications
World Health Organization (2005) Recommendations for the production, control and regulation of human plasma for fractionation, Annex 4, TRS nº 941, pp. 69.
EMA/CHMP/BPWP/94033/2007 rev. 4. Guideline on the clinical investigation of human normal immunoglobulin for intravenous administration (IVIg), Sep,2020.
Brasil, Resolução nº 251, de 07 de agosto de 1977. Disponível em; https://www.inca.gov.br/sites/ufu.sti.inca.local/files//media/document//resolucao-cns-251-97.pdf. Acesso em 25 de out de 2023
Food and Drug Administration (2006). Guidance for Clinical Trial Sponsors on the Establishment and Operation of Clinical Trial Data Monitoring Committees. Rockville, MD, pp. 38.
Study at a glance
From the registry record, last updated by the sponsor on 3 Jun 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Evaluating the Safety, Effectiveness, and Pharmacokinetics of Boya Intravenous Immune Globulin in Patients With Primary Immune Deficiency.
- ClinicalTrials.gov ID
- NCT06150833
- Acronym / sponsor ID
- BoyaIVIG / BoyaIVIG
- Conditions
- Primary Immunodeficiency Disease
- Keywords
- IVIG, primary immunodeficiency disease, PID, common variable immunodeficiency, CVID, X-linked agammaglobulinemia, XLA
- Phase
- Phase 3
- Study type
- Interventional
- Recruitment status
- Not yet recruiting
- Enrolment
- 50 participants (estimated)
- Lead sponsor
- Azidus BrasilIndustry (pharma, biotech, devices)
- Collaborators
- Boya Bio Pharmaceutical Group Co Ltd
- Study start
- Sep 2026 (estimated)
- Primary completion
- Sep 2028 (estimated)
- Study completion
- Sep 2028 (estimated)
- First posted
- 29 Nov 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The goal of this phase 3, open-label, single-group clinical trial is to assess the efficacy of Boya IVIG in maintaining the mean number of serious bacterial infections to less than one per year in participants with primary immunodeficiency (PYD) due to common variable immunodeficiency (CVID), as defined by the European Immunodeficiency Society (ESCID) / Pan American Immunodeficiency Group (PAGID), or X-linked agammaglobulinemia (XLA), as defined by molecular genetic testing (ESCID/PAGID).
The safety and pharmacokinetics (PK) of the investigational product will also be evaluated.
Participants must:
- Visit the research center every 21 or 28 days to receive the experimental product infusion and undergo a medical examination.
- During weekly telephone calls, report, if applicable, adverse events and hospitalizations; the number of school or workdays missed due to infections; the length of hospital stay; and the use of antibiotics for therapeutic purposes.
Detailed description
Fifty male or female participants aged 2 to 60 years, either treatment-naive or already receiving intravenous immunoglobulin replacement therapy, will be enrolled, including at least 20 participants aged 2 to 17 years. The study will also examine the pharmacokinetic (PK) profile in adult participants.
After obtaining signed informed consent or assent, screening will include reviewing immunodeficiency history in medical records, performing safety examinations, and assessing eligibility against inclusion and exclusion criteria.
Subjects who pass screening will begin a 6-visit run-in period. For participants already receiving treatment, the interval between intravenous injections should remain as prescribed before enrollment unless modified during the run-in period. During this period, participants will receive the study IVIG. For treatment-naïve participants, the dose and administration interval during the run-in will be determined by the Investigator.
After the run-in, the one-year trial will begin at V0. Study visits will be scheduled every 21 or 28 days, based on the participant's prescribed treatment plan. Each visit will have a ±3-day window around the scheduled date. At each visit, blood samples will be collected immediately before each IVIG dose to measure IgG trough levels. If a visit occurs earlier or later than the scheduled date, whether within or outside the allowed window, the timing of the next visit will be based on the actual date of the previous visit to maintain consistent planned inter-visit intervals throughout the study.
The V0 assessment will begin when participants have IgG concentrations ≥5 g/L on two consecutive infusions under the same dosing conditions. Therefore, the run-in period may include only two visits. If, among the six visits, the trough IgG concentration does not reach 5 g/L on two consecutive visits, the participant will be considered to have failed screening but may be rescreened.
To characterize the pharmacokinetic (PK) profile of the investigational product, at least 20 adult participants will undergo additional blood sampling between two consecutive study visits to measure total IgG concentrations and antigen-specific antibody levels, including anti-pneumococcal capsular polysaccharide, anti-Haemophilus influenzae, and anti-measles antibodies.
PK sampling should preferably be performed at Visit 4 (V4), provided that a stable dosing regimen has been maintained. Participants receiving IVIG on a 21-day schedule should collect seven samples at 30 minutes, 2 hours, 24 hours, 72 hours, 7 days, 14 days, and 21 days post-infusion. Participants receiving IVIG on a 28-day schedule should collect eight additional samples at 30 minutes, 2 hours, 24 hours, 72 hours, 14 days, 21 days, and 28 days post-infusion.
The PK profile should be evaluated only after at least four consecutive dosing intervals with no changes in posology, meaning both the dose and dosing interval remain unchanged, preferably at Visit 4 (V4). If any dose or interval adjustments occur between V0 and V4, PK profile sampling should be delayed until the next visit, after dosage stability is confirmed.
Participants will be contacted weekly between infusions to collect data on adverse events, concomitant medications, duration of infection treatment, and time lost from work or school due to infections during the period.
Additionally, subjects will have continued access to the investigator's team to report adverse events and to receive advice on next steps or additional medical evaluations, if necessary.
Medical evaluation, vital signs, and oximetry, adverse events, and concomitant medication will be assessed at all visits.
Safety laboratory tests (including direct Coombs and pregnancy tests) will be performed at every 4th or 5th visit.
Study design
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
- Model description
- Patients with primary immunodeficiency will start therapy or switch to Boya IVIG and optimize the posology in a run-in period of 2 to 6 administrations. In the one-year test period, the patients will receive the test IVIG at 21- or 28-day intervals and be followed. IgG trough levels will be collected from all participants, at all visits. The pharmacokinetic profile will be measured after 5 infusions with stable dose in 20 adult participants, collecting additional blood samples.
| Arm | Type | Receives |
|---|---|---|
| Boya IVIG | Experimental | Biological: Boya IVIGAll participants will receive Boya IVIG: Dose: 200 to 800 mg/kg Schedule of administration: 21- or 28-day interval Time frame: 54 weeks (21-day interval) or 56 weeks (28-day interval) |
Who may qualify
- Ages
- 2 to 60 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult
Key inclusion criteria (41 listed)
- Men or women; age between 02 and 60 years; written informed consent/assent.
- Diagnosis of primary immunodeficiency disease (PID) with decreased antibody production due to common variable immunodeficiency (CVID) or X-linked agammaglobulinemia (XLA).
- Treatment-naïve patients and those receiving intravenous immunoglobulin replacement therapy at 21- to 28-day intervals, with doses ranging from 300 to 800 mg/kg per infusion.
- Negative pregnancy test in females of childbearing potential; willingness to use effective contraceptive methods throughout the study.
- Subjects currently receiving any subcutaneous or intramuscular immunoglobulin may be enrolled by switching to IVIG therapy at the investigator's discretion, considering the potential benefit to the participant.
Key exclusion criteria (0 listed)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Boya IVIGAlso: IVIG, BOYAIntervention: Biological: Boya IVIG Boya IVIG is a 5% human immunoglobulin for intravenous administration | Biological | Boya IVIG |
Primary outcome
Primary Efficacy Objective
Time frame: 54 weeks (21-day interval schedule) or 56 weeks (28-day interval schedule)
Average incidence of serious bacterial infections per participant between V0 and Vfinal.
4 secondary outcomes
Assessment of the rate of non-serious infections within one year
Time frame: Average incidence of non-serious infections per patient between Visit 0 and Final Visit (through study completion, an average of 1 year), as documented as treatment emergent adverse events (TEAEs).
Missing time from school/work
Time frame: Average number of days off from school/work per patient/year, as collected in weekly telephone contacts.
Length of hospitalization
Time frame: Number of days of hospitalization due to infections per participant/year between V0 and Vfinal, as documented as Adverse Events.
Use of antibiotics
Time frame: Tabulation of all antibiotics used, separating those indicated for prophylactic and therapeutic purposes
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 3 Jun 2026.
- BackgroundWorld Health Organization (2005) Recommendations for the production, control and regulation of human plasma for fractionation, Annex 4, TRS nº 941, pp. 69.
- BackgroundEMA/CHMP/BPWP/94033/2007 rev. 4. Guideline on the clinical investigation of human normal immunoglobulin for intravenous administration (IVIg), Sep,2020.
- BackgroundBrasil, Resolução nº 251, de 07 de agosto de 1977. Disponível em; https://www.inca.gov.br/sites/ufu.sti.inca.local/files//media/document//resolucao-cns-251-97.pdf. Acesso em 25 de out de 2023
- BackgroundFood and Drug Administration (2006). Guidance for Clinical Trial Sponsors on the Establishment and Operation of Clinical Trial Data Monitoring Committees. Rockville, MD, pp. 38.
- Individual participant dataSharing planned: No. It is believed that after the data analysis and presentation to the National Commission on Research Ethics, all data of the study will become public.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Luciana Ferrara study director
Azidus Brasil
Questions about this trial
What is this clinical trial studying?
A Phase 3 study testing Boya IVIG in people with Primary Immunodeficiency Disease, run by Azidus Brasil.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 41 inclusion and 0 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: opening soon, as of the sponsor's last update on 3 Jun 2026. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Luciana Ferrara (+55 19 981428814, luciana.ferrara@azidusbrasil.com.br), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Primary Efficacy Objective (time frame: 54 weeks (21-day interval schedule) or 56 weeks (28-day interval schedule)). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT06150833, which also lists 4 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 3 Jun 2026.