Cervical Intraepithelial Neoplasia Grade 1Phase 1/2NCT07809997
Phase I/II Trial of Electroporation-Delivered pBI-4 Vaccine (TriGrid™ PVX4) for Treatment of Women With HPV16-Positive CIN1 or Persistent Infection
A Phase 1/2 study testing pBI-4 Vaccine in people with Cervical Intraepithelial Neoplasia Grade 1 and Human Papillomavirus 16 Infection, run by Chang Gung Memorial Hospital at 2 sites in Taiwan.
Trial summary
The purpose of this study is to evaluate the safety, efficacy, and tolerability of pBI-4, an investigational therapeutic DNA vaccine, in treating adult women with Human Papillomavirus type 16 (HPV16)-positive Grade 1 cervical intraepithelial neoplasia (CIN1) or persistent HPV16 infection. Read more about this study
- Who is it for?
- Ages 19 to 65 years, women only
- Conditions the study is for
- Cervical Intraepithelial Neoplasia Grade 1, Human Papillomavirus 16 Infection
- What is being tested?
- pBI-4 Vaccine
- Type of treatment
- Vaccines, Injection or infusion
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 94 participants
- Where
- 2 sitesTaiwan
- Study dates
- Sep 2026to Mar 2030
- Phase
- Phase 1/2
- 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 19 to 65 years
- Women only
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Patients with CIN1 on biopsy and whose cytologic sample is HPV16+ by Roche Cobas test in the past 30 days, OR patients with CIN<1 on biopsy whose cytologic sample is HPV16+ by Roche Cobas test in the past 30 days and a history of a second HPV16+ test at least 6 months prior
- (Co-infections with HPV types other than HPV16 are permissible for study entry)
- Age ≥ 19 years
- Baseline Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1 at the time of study treatment administration
- Adequate organ function at the time of enrollment as defined by:
- White blood cell count > 3,000/mcL Absolute lymphocyte number > 500/mcL Absolute neutrophil count > 1,000/mcL Platelets > 90,000/mcL Hemoglobin > 9 g/dL Total bilirubin < 3 x institutional limit of normal AST(SGOT)/ALT(SGPT) < 3 x institutional limit of normal Creatinine < 2.5 x institutional limit of normal Women of child-bearing potential must agree to use effective contraception (hormonal and/or barrier) prior to study entry and for the duration of the study
- Ability to understand and willingness to sign a written informed consent document
- Subject is able to adhere to the study visit schedule and other protocol requirements
Who cannot join
- Patients with AIS (adenocarcinoma in situ) or cancer determined by cervical cytology at study entry
- Histologic evidence of CIN2 or above
- Patients with a diagnosis of immunosuppression or prolonged, active use of immunosuppressive medications such as steroids
- Prior treatment with any HPV therapeutic agent (e.g., Imiquimod, Veregen, Podophylotoxin)
- Patients who are receiving any other investigational agents or blood products within 30 days prior to the first dose
- Patients with an uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance
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- Patients with a history of autoimmune disease such as multiple sclerosis (exclusive of a history of thyroiditis, psoriasis, Sjogren's, or inflammatory bowel disease)
- Patients with a history of allergic reactions attributed to compounds used in agent preparation
- Patients who are pregnant or breast feeding
- Patients with active or chronic infection of HIV, HCV, or HBV
- Patients who have had a prior LEEP or cervical conization procedure
- History of prior malignancy (permitted only if the patient has been disease-free for ≥ 5 years, or has completely resected basal cell or squamous cell carcinoma of the skin)
- Less than 1 acceptable potential injection site for intramuscular injection and electroporation (considering the left/right medial deltoid, and anterolateral quadriceps muscles)
- A site is unacceptable if there is inadequate muscle mass to support at least a 19 mm (0.75 inch) injection depth or a skinfold thickness of ≥ 50 mm
- (Note: For participants weighing ≤ 65 kg, acceptable sites are confined to the outer aspect of the upper thigh, and the deltoids are not eligible)
- Contraindication to intramuscular injections and blood draws
- A metal implant or implantable device within the area of the electroporation injection site at > 2 of the eligible injection sites .A nonremovable electronic stimulation device (such as cardiac demand pacemakers, automatic implantable cardiac defibrillators, nerve stimulators, or deep brain stimulators).
Trial locations and contacts
2 sites in 1 country. Contact the study team or a site near you to ask about taking part.
Taiwan2 sites
Kaohsiung Chang Gung Memorial Hospital
Kaohsiung City, Kaohsiung, 833
Hao Lin, MD, 886-7-7317123 ext. 8914, haolin@cgmh.org.tw
Linkou Chang Gung Memorial Hospital
Taoyuan, Taoyuan, 333
Angel Chao, Ph.D., 886-3-3281200 ext.8983, angel945@cgmh.org.tw
About this study
Official title: A Randomized, Double-Blind, Placebo-Controlled Phase II Trial of pBI-4 Plasmid Administered Via Intramuscular TriGrid™ Electroporation Delivery System for Treatment of Women With HPV16-Positive Grade 1 Cervical Intraepithelial Neoplasia or Persistent HPV16 Infection
The purpose of this study is to evaluate the safety, efficacy, and tolerability of pBI-4, an investigational therapeutic DNA vaccine, in treating adult women with Human Papillomavirus type 16 (HPV16)-positive Grade 1 cervical intraepithelial neoplasia (CIN1) or persistent HPV16 infection.
This is a randomized, double-blind, placebo-controlled, multicenter Phase II trial in Taiwan, aiming to enroll a total of 94 female participants. Participants will be randomly assigned (1:1 ratio) to receive either a single 1.0 mg dose of the pBI-4 vaccine or a placebo. The study drug or placebo will be administered intramuscularly in the thigh muscle using the TriGrid™ Delivery System version 2.0 (TDS-IM v2.0), a specialized device that applies short, mild electrical pulses (electroporation) to help cells take up the vaccine and stimulate a stronger immune response.
The primary goal of the study is to compare the rate of HPV16 viral clearance between the vaccine and placebo groups at Month 6. The study also features an adaptive design: an interim analysis will be conducted after approximately 50% of participants complete their 6-month assessment. If the initial single-dose regimen shows suboptimal efficacy at the interim stage, the trial may adaptively switch to a two-dose (prime-boost) regimen administered one month apart for the remaining participants. All participants will be closely monitored for safety, side effects, and immune responses for a total duration of 12 months.
Read the detailed description
STUDY OVERVIEW AND TRIAL DESIGN This study is a randomized, double-blind, placebo-controlled, multicenter Phase II clinical trial in Taiwan to evaluate the safety, efficacy, tolerability, and immunogenicity of the pBI-4 therapeutic DNA vaccine administered via the clinical-stage Intramuscular TriGrid™ Delivery System version 2.0 (TDS-IM v2.0) [1-4]. The target study population consists of adult female subjects aged 19 years and older who have biopsy-confirmed Grade 1 cervical intraepithelial neoplasia (CIN1) with concurrent Human Papillomavirus type 16 (HPV16) infection, or who exhibit persistent (defined as 6 months or longer) HPV16 infection with normal cytology (CIN<1) [5-8].
A maximum target of 94 eligible subjects will be enrolled and randomized in a 1:1 ratio into two parallel groups: 47 subjects in the active pBI-4 vaccine group and 47 subjects in the placebo group [1, 4, 9].
THERAPEUTIC VACCINE AND ELECTROPORATION DELIVERY MECHANISM The investigational drug, pBI-4, is a clinical-grade, 6,999 base-pair circular plasmid DNA vaccine [10-12]. It is engineered to express human calreticulin (CRT) linked to codon-optimized HPV16 E6, E7, and L2 residues (amino acids 11-200) [11]. To ensure clinical safety, the gene sequences encoding the HPV16 E6 and E7 proteins incorporate specific mutations that disable their native oncogenic functions [10, 11, 13].
The vaccine (at a dose of 1.0 mg in 1.0 mL volume) or placebo (1.0 mL of phosphate-buffered saline) is administered intramuscularly into the vastus lateralis (thigh) muscle [1, 14, 15]. To overcome the historical limitation of low cellular DNA uptake in humans, the trial utilizes the automated TDS-IM v2.0 delivery system [14, 16-18]. During the automated administration sequence (which takes approximately 10 seconds), the device deploys an injection needle and four surrounding electrodes into the muscle [19]. Following fluid delivery, short, mild electrical pulses are applied to the local tissue [19]. This electroporation process transiently opens pores in cell membranes, enhancing intracellular plasmid DNA uptake and antigen expression by 2 to 3 orders of magnitude compared to standard needle injections [16, 19, 20].
TWO-STAGE ADAPTIVE REGIMEN MODIFICATION The trial employs a two-stage group-sequential design featuring a pre-specified, non-binding adaptive regimen modification [3, 21]. A single interim analysis will be conducted by an independent Data Safety Monitoring Board (DSMB) once approximately 50% of the randomized participants (approximately 42 patients) complete their Month 6 primary assessment [9, 22].
At the interim analysis, the DSMB will calculate the conditional power (CP) based on the primary efficacy endpoint (HPV16 clearance rate) under the design alternative (assuming a 60% clearance rate in the vaccine group versus a 30% clearance rate in the placebo group) [9, 21, 23].
- If the conditional power is calculated to be less than 20% (indicating suboptimal efficacy of the single-dose regimen), the trial will trigger a non-binding futility rule and adaptively switch to a two-dose (prime-boost) regimen for all remaining participants enrolled in Stage 2 [21]. Under this adapted schedule, Stage 2 participants will receive their first dose at Month 0 and a booster dose at Month 2, while maintaining double-blind placebo control and 1:1 randomization [21, 24].
- If the conditional power is 20% or higher, the trial will continue with the original single-dose regimen for the rest of the study [21].
CLINICAL EVALUATIONS AND FOLLOW-UP TIMELINE
All participating subjects will undergo structured clinical assessments across multiple visits:
- Baseline/Screening (Month -1 to 0): Obtaining written informed consent, checking full eligibility, medical and gynecological history, physical examination with ECOG performance status, vital signs, clinical laboratory tests (including complete blood count with differential, serum chemistry, HIV, Hepatitis B and C screenings), urine pregnancy test, Pap smear, Roche Cobas HPV genotyping, and colposcopy with endocervical curettage (ECC) and mandatory tissue biopsy [6, 25-27].
- Vaccination Visit (Month 0 Day 1): Pre-dose physical exam, vital signs, urine pregnancy test, and a research blood draw (serum and peripheral blood mononuclear cells) for baseline HPV16-specific humoral and cell-mediated immune assessments [14, 28-30]. Following the pBI-4 or placebo injection via TDS-IM v2.0, subjects are observed on-site for up to 60 minutes, with vital signs recorded at 30 and 60 minutes post-dose to monitor for potential immediate hypersensitivity or vasovagal reactions [14, 30-32].
- Post-Vaccination Phone Call (Week 1 / Day 8): A telephone interview to record any local reactogenicity, systemic adverse events, and concomitant medications, alongside the administration of the Procedure Tolerability Questionnaire to measure pain (using a 10-point Visual Analog Scale) and device acceptability [29, 31-33].
- Month 6 Follow-Up Visit: Physical exam, vital signs, safety laboratory tests, research blood draw for immunologic response, Pap smear, Roche Cobas HPV genotyping, and colposcopy with ECC (with biopsy performed only if clinically indicated) [29, 34-36].
- Month 12 Follow-Up Visit (Final Evaluation): A replication of the Month 6 visit assessments, representing the completion of the 12-month post-vaccination follow-up period.
If the adaptive two-dose regimen is triggered, Stage 2 participants will undergo an additional vaccination visit at Month 2 Day 1 (with pre-dose safety labs and a pregnancy test) and a subsequent post-vaccination telephone call at Week 9 to document tolerability and safety parameters [24, 40].
- Being tested
- pBI-4 Vaccine
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
pBI-4 VaccineBiological
A clinical-grade, 6,999 base-pair circular recombinant plasmid DNA vaccine (pBI-4) engineered to express human calreticulin (CRT) linked to codon-optimized HPV16 E6, E7, and L2 residues (amino acids 11-200). To ensure clinical safety, E6 and E7 incorporate inactivating mutations to disable their native oncogenic transforming activities. Administered at a dose of 1.0 mg (1.0 mL) intramuscularly into the thigh muscle using the TDS-IM v2.0 electroporation device.
| Study group | Role | What they receive |
|---|---|---|
| pBI-4 Vaccine | Experimental | A clinical-grade, 6,999 base-pair circular recombinant plasmid DNA vaccine (pBI-4) engineered to express human calreticulin (CRT) linked to codon-optimized HPV16 E6, E7, and L2 residues (amino acids 11-200). To ensure clinical safety, E6 and E7 incorporate inactivating mutations to disable their native oncogenic transforming activities. Administered at a dose of 1.0 mg (1.0 mL) intramuscularly into the thigh muscle using the TDS-IM v2.0 electroporation device. Receives: Biological: pBI-4 Vaccine |
| Placebo | Placebo comparator | Placebo Receives: Biological: pBI-4 Vaccine |
What is being measured
The primary outcome is the main question the study is designed to answer.
Proportion of subjects exhibiting virological clearance of HPV16 and histopathological regression of cervical lesions to < CIN2 at Month 6
The proportion of subjects with histopathologically confirmed HPV16-associated CIN2 or CIN3 who exhibit virological clearance of HPV16 and regression of cervical lesions to < CIN2 at Month 6.
Measured: Month 6 (or 6 months post-vaccination)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted9 Sep 2026
- Study startSep 2026 (estimated)
- Primary completionMar 2030 (estimated)
- Study completionMar 2030 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Cervical Intraepithelial Neoplasia Grade 1Studies of the same condition, open and under way.
- More trials run by Chang Gung Memorial HospitalThe sponsor's other registered studies.
- 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 1/2
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind
- Who is masked
- Participant, Care provider, Investigator, Outcomes assessor
- Enrolment
- 94 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Chang Gung Memorial Hospital
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Chao, Angel, Chang Gung Memorial Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07809997
- Sponsor's protocol ID
- TGOG1018
- Status last verified
- Sep 2026
- First submitted
- 11 Aug 2026
- Last updated
- 14 Sep 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: No individual participant data will be shared with persons other than the investigators of this study to protect participant confidentiality.
Study at a glance
From the registry record, last updated by the sponsor on 14 Sep 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Randomized, Double-Blind, Placebo-Controlled Phase II Trial of pBI-4 Plasmid Administered Via Intramuscular TriGrid™ Electroporation Delivery System for Treatment of Women With HPV16-Positive Grade 1 Cervical Intraepithelial Neoplasia or Persistent HPV16 Infection
- ClinicalTrials.gov ID
- NCT07809997
- Acronym / sponsor ID
- TGOG1018
- Phase
- Phase 1/2
- Study type
- Interventional
- Recruitment status
- Not yet recruiting
- Enrolment
- 94 participants (estimated)
- Lead sponsor
- Chang Gung Memorial HospitalUniversity, hospital or other
- Study start
- Sep 2026 (estimated)
- Primary completion
- Mar 2030 (estimated)
- Study completion
- Mar 2030 (estimated)
- First posted
- 9 Sep 2026 (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 purpose of this study is to evaluate the safety, efficacy, and tolerability of pBI-4, an investigational therapeutic DNA vaccine, in treating adult women with Human Papillomavirus type 16 (HPV16)-positive Grade 1 cervical intraepithelial neoplasia (CIN1) or persistent HPV16 infection.
This is a randomized, double-blind, placebo-controlled, multicenter Phase II trial in Taiwan, aiming to enroll a total of 94 female participants. Participants will be randomly assigned (1:1 ratio) to receive either a single 1.0 mg dose of the pBI-4 vaccine or a placebo. The study drug or placebo will be administered intramuscularly in the thigh muscle using the TriGrid™ Delivery System version 2.0 (TDS-IM v2.0), a specialized device that applies short, mild electrical pulses (electroporation) to help cells take up the vaccine and stimulate a stronger immune response.
The primary goal of the study is to compare the rate of HPV16 viral clearance between the vaccine and placebo groups at Month 6. The study also features an adaptive design: an interim analysis will be conducted after approximately 50% of participants complete their 6-month assessment. If the initial single-dose regimen shows suboptimal efficacy at the interim stage, the trial may adaptively switch to a two-dose (prime-boost) regimen administered one month apart for the remaining participants. All participants will be closely monitored for safety, side effects, and immune responses for a total duration of 12 months.
Detailed description
STUDY OVERVIEW AND TRIAL DESIGN This study is a randomized, double-blind, placebo-controlled, multicenter Phase II clinical trial in Taiwan to evaluate the safety, efficacy, tolerability, and immunogenicity of the pBI-4 therapeutic DNA vaccine administered via the clinical-stage Intramuscular TriGrid™ Delivery System version 2.0 (TDS-IM v2.0) [1-4]. The target study population consists of adult female subjects aged 19 years and older who have biopsy-confirmed Grade 1 cervical intraepithelial neoplasia (CIN1) with concurrent Human Papillomavirus type 16 (HPV16) infection, or who exhibit persistent (defined as 6 months or longer) HPV16 infection with normal cytology (CIN<1) [5-8].
A maximum target of 94 eligible subjects will be enrolled and randomized in a 1:1 ratio into two parallel groups: 47 subjects in the active pBI-4 vaccine group and 47 subjects in the placebo group [1, 4, 9].
THERAPEUTIC VACCINE AND ELECTROPORATION DELIVERY MECHANISM The investigational drug, pBI-4, is a clinical-grade, 6,999 base-pair circular plasmid DNA vaccine [10-12]. It is engineered to express human calreticulin (CRT) linked to codon-optimized HPV16 E6, E7, and L2 residues (amino acids 11-200) [11]. To ensure clinical safety, the gene sequences encoding the HPV16 E6 and E7 proteins incorporate specific mutations that disable their native oncogenic functions [10, 11, 13].
The vaccine (at a dose of 1.0 mg in 1.0 mL volume) or placebo (1.0 mL of phosphate-buffered saline) is administered intramuscularly into the vastus lateralis (thigh) muscle [1, 14, 15]. To overcome the historical limitation of low cellular DNA uptake in humans, the trial utilizes the automated TDS-IM v2.0 delivery system [14, 16-18]. During the automated administration sequence (which takes approximately 10 seconds), the device deploys an injection needle and four surrounding electrodes into the muscle [19]. Following fluid delivery, short, mild electrical pulses are applied to the local tissue [19]. This electroporation process transiently opens pores in cell membranes, enhancing intracellular plasmid DNA uptake and antigen expression by 2 to 3 orders of magnitude compared to standard needle injections [16, 19, 20].
TWO-STAGE ADAPTIVE REGIMEN MODIFICATION The trial employs a two-stage group-sequential design featuring a pre-specified, non-binding adaptive regimen modification [3, 21]. A single interim analysis will be conducted by an independent Data Safety Monitoring Board (DSMB) once approximately 50% of the randomized participants (approximately 42 patients) complete their Month 6 primary assessment [9, 22].
At the interim analysis, the DSMB will calculate the conditional power (CP) based on the primary efficacy endpoint (HPV16 clearance rate) under the design alternative (assuming a 60% clearance rate in the vaccine group versus a 30% clearance rate in the placebo group) [9, 21, 23].
- If the conditional power is calculated to be less than 20% (indicating suboptimal efficacy of the single-dose regimen), the trial will trigger a non-binding futility rule and adaptively switch to a two-dose (prime-boost) regimen for all remaining participants enrolled in Stage 2 [21]. Under this adapted schedule, Stage 2 participants will receive their first dose at Month 0 and a booster dose at Month 2, while maintaining double-blind placebo control and 1:1 randomization [21, 24].
- If the conditional power is 20% or higher, the trial will continue with the original single-dose regimen for the rest of the study [21].
CLINICAL EVALUATIONS AND FOLLOW-UP TIMELINE
All participating subjects will undergo structured clinical assessments across multiple visits:
- Baseline/Screening (Month -1 to 0): Obtaining written informed consent, checking full eligibility, medical and gynecological history, physical examination with ECOG performance status, vital signs, clinical laboratory tests (including complete blood count with differential, serum chemistry, HIV, Hepatitis B and C screenings), urine pregnancy test, Pap smear, Roche Cobas HPV genotyping, and colposcopy with endocervical curettage (ECC) and mandatory tissue biopsy [6, 25-27].
- Vaccination Visit (Month 0 Day 1): Pre-dose physical exam, vital signs, urine pregnancy test, and a research blood draw (serum and peripheral blood mononuclear cells) for baseline HPV16-specific humoral and cell-mediated immune assessments [14, 28-30]. Following the pBI-4 or placebo injection via TDS-IM v2.0, subjects are observed on-site for up to 60 minutes, with vital signs recorded at 30 and 60 minutes post-dose to monitor for potential immediate hypersensitivity or vasovagal reactions [14, 30-32].
- Post-Vaccination Phone Call (Week 1 / Day 8): A telephone interview to record any local reactogenicity, systemic adverse events, and concomitant medications, alongside the administration of the Procedure Tolerability Questionnaire to measure pain (using a 10-point Visual Analog Scale) and device acceptability [29, 31-33].
- Month 6 Follow-Up Visit: Physical exam, vital signs, safety laboratory tests, research blood draw for immunologic response, Pap smear, Roche Cobas HPV genotyping, and colposcopy with ECC (with biopsy performed only if clinically indicated) [29, 34-36].
- Month 12 Follow-Up Visit (Final Evaluation): A replication of the Month 6 visit assessments, representing the completion of the 12-month post-vaccination follow-up period.
If the adaptive two-dose regimen is triggered, Stage 2 participants will undergo an additional vaccination visit at Month 2 Day 1 (with pre-dose safety labs and a pregnancy test) and a subsequent post-vaccination telephone call at Week 9 to document tolerability and safety parameters [24, 40].
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind (participant, care provider, investigator, outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| pBI-4 Vaccine | Experimental | Biological: pBI-4 VaccineA clinical-grade, 6,999 base-pair circular recombinant plasmid DNA vaccine (pBI-4) engineered to express human calreticulin (CRT) linked to codon-optimized HPV16 E6, E7, and L2 residues (amino acids 11-200). To ensure clinical safety, E6 and E7 incorporate inactivating mutations to disable their native oncogenic transforming activities. Administered at a dose of 1.0 mg (1.0 mL) intramuscularly into the thigh muscle using the TDS-IM v2.0 electroporation device. |
| Placebo | Placebo comparator | Biological: pBI-4 VaccinePlacebo |
Who may qualify
- Ages
- 19 to 65 years
- Sex
- Female only
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (8 listed)
- Patients with CIN1 on biopsy and whose cytologic sample is HPV16+ by Roche Cobas test in the past 30 days, OR patients with CIN<1 on biopsy whose cytologic sample is HPV16+ by Roche Cobas test in the past 30 days and a history of a second HPV16+ test at least 6 months prior
- White blood cell count > 3,000/mcL Absolute lymphocyte number > 500/mcL Absolute neutrophil count > 1,000/mcL Platelets > 90,000/mcL Hemoglobin > 9 g/dL Total bilirubin < 3 x institutional limit of normal AST(SGOT)/ALT(SGPT) < 3 x institutional limit of normal Creatinine < 2.5 x institutional limit of normal Women of child-bearing potential must agree to use effective contraception (hormonal and/or barrier) prior to study entry and for the duration of the study
- Ability to understand and willingness to sign a written informed consent document
- Subject is able to adhere to the study visit schedule and other protocol requirements
Key exclusion criteria (17 listed)
- Patients with AIS (adenocarcinoma in situ) or cancer determined by cervical cytology at study entry
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 |
|---|---|---|
| pBI-4 VaccineA clinical-grade, 6,999 base-pair circular recombinant plasmid DNA vaccine (pBI-4) engineered to express human calreticulin (CRT) linked to codon-optimized HPV16 E6, E7, and L2 residues (amino acids 11-200). To ensure clinical safety, E6 and E7 incorporate inactivating mutations to disable their native oncogenic transforming activities. Administered at a dose of 1.0 mg (1.0 mL) intramuscularly into the thigh muscle using the TDS-IM v2.0 electroporation device. | Biological | Placebo, pBI-4 Vaccine |
Primary outcome
Proportion of subjects exhibiting virological clearance of HPV16 and histopathological regression of cervical lesions to < CIN2 at Month 6
Time frame: Month 6 (or 6 months post-vaccination)
The proportion of subjects with histopathologically confirmed HPV16-associated CIN2 or CIN3 who exhibit virological clearance of HPV16 and regression of cervical lesions to < CIN2 at Month 6.
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 14 Sep 2026.
- Individual participant dataSharing planned: No. No individual participant data will be shared with persons other than the investigators of this study to protect participant confidentiality.
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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.
2 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 1/2 study testing pBI-4 Vaccine in people with Cervical Intraepithelial Neoplasia Grade 1 and Human Papillomavirus 16 Infection, run by Chang Gung Memorial Hospital at 2 sites in Taiwan.
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 8 inclusion and 17 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 14 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 2 sites in Taiwan. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this combined phase mean?
Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.
Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
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 Angel Chao, MD, PhD (+886-975365884, drangiechao@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Proportion of subjects exhibiting virological clearance of HPV16 and histopathological regression of cervical lesions to < CIN2 at Month 6 (time frame: Month 6 (or 6 months post-vaccination)). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
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 14 Sep 2026.