ImQuest (IQP) DuoGel Phase 1 Pharmacokinetic Study

Johns Hopkins University

Status and phase

Completed

Phase 1

Conditions

HIV Prevention

Treatments

Drug: DuoGel

Study type

Interventional

Funder types

Other

Industry

NIH

Identifiers

NCT03082690

IRB00041089

5U19AI101961 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

The purpose of this study is describe the safety and single-dose pharmacokinetics of rectally-administered IQP (ImQuest Pharmaceuticals)-0528 (DuoGel) in plasma, rectal tissue biopsies, vaginal tissue biopsies, rectal fluid and cervicovaginal fluid as well as to assess the luminal distribution of IQP-0528 in the rectum. Sixteen healthy volunteers will receive a single rectal dose of DuoGel, followed by blood, tissue and fluid sampling over the following 72 hours.

Full description

This is a phase 1 open label study of the safety, PK, and PD of single-dose 10 mL IQP-0528 through rectal administration. Pharmacokinetics (PK) will be assessed in multiple compartments: plasma, rectal tissue, vaginal tissue, rectal fluid and cervicovaginal fluid. The luminal distribution of DuoGel in the rectum will be evaluated with Single Photon Emission Computed Tomography/ X-ray Computed Tomography (SPECT/CT). Pharmacodynamics (PD) will be assessed in an ex vivo HIV explant challenge of rectal and vaginal tissue biopsies.

After completing the screening evaluation (Visit 1) and establishing participant eligibility, 16 eligible participants will be enrolled: 8 men and 8 women. A subsequent baseline visit (Visit 2) safety assessment and tissue ex vivo HIV explant challenge will be performed as baseline for comparison with later post-drug evaluation. Participants will receive a single 10 mL rectal dose of 99mTechnetium (99mTc) -radiolabelled DuoGel (Visit 3), followed by safety assessments and PK and PD sampling over three days (Visits 3, 4, and 5). Finally, a follow-up safety phone call is performed a week after all PK sampling and biopsies are collected.

Enrollment

10 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

18 years or older at screening
HIV-1 negative as documented at screening
Willing to use condoms for the duration of the study
Willing to refrain from aspirin and non-steroidal anti-inflammatory drug (NSAID) use for one week before and after each study biopsy visit
Available to return for all study visits
Agrees to sexually transmitted infection (STI) reporting requirements
Able and willing to communicate in English
Able and willing to provide written informed consent
Able and willing to provide adequate information for locator purposes
Agrees not to participate in other research studies
Willing to refrain from receptive anal intercourse and insertion of anything in the rectum for 72 hours before and after rectal biopsies.

Additional inclusion criteria for women:

Be pre-menopausal
Have regular menstrual cycles (unless on contraception that causes amenorrhea or irregular menses)
Have a negative qualitative urine pregnancy test
Per participant report, using an effective method of contraception at enrollment; hormonal method (except vaginal ring) used continuously for the past 30 days; intrauterine device (IUD [copper or hormonal] inserted at least 30 days prior to enrollment); female sterilization; abstinent from sexual activity with male partner for the past 30 days; or sexual activity with vasectomized partner; and willingness to use effective method of contraception until the completion of final scheduled study visit if enrolled.
Willing to refrain from insertion of anything into the vagina for at least 72 hours before and 7 days after vaginal biopsies.

Exclusion criteria

Current known HIV-infected partners
Current use of anticoagulant medications associated with increased risk for bleeding following mucosal biopsy (e.g., daily high dose aspirin [>81 mg], NSAIDs, or Pradaxa®)
Current use of cytochrome P450 3A (CYP3A) inducer(s) and/or inhibitor(s)
Use of systemic immunomodulatory medications within 4 weeks of enrollment
Known allergic reaction to components of the study product
History of recurrent urticaria
Participants whose whole body radiation exposure exceeds 5000 millirem (mRem)/year.
Participants who are currently receiving or have been on oral PrEP or PEP in the past month
Any other clinical condition or prior therapy that, in the opinion of the investigator, would make the patient unsuitable for the study or unable to comply with the study requirements.
Significant colorectal symptom(s) as determined by medical history or by participant self-report
Active rectal infection, requiring treatment per current Centers for Disease Control (CDC) guidelines or symptomatic urinary tract infection (UTI). Infections requiring treatment include Chlamydia (CT), gonorrhea (GC), syphilis, active herpes simplex virus (HSV) lesions, chancroid, genital sores or ulcers, and, if clinically indicated, genital warts.
History of STI within the last 3 months.
Use of post-exposure (PEP) or pre-exposure (PrEP) prophylaxis within the last 6 months
History of significant gastrointestinal bleeding
Use of any rectally administered medications within 4 weeks of enrollment or unwillingness to refrain from use of any rectally administered medications 72 hours prior to any study dosing or biopsy visit
Use of any rectally administered products containing nonoxynol-9 (including condoms) or investigational products within 4 weeks of enrollment

Additional exclusion criteria for women:

Significant vaginal symptoms, genital lesions, erythema, edema or any other abnormal physical finding that, in the opinion of the investigator or designee, would contraindicate study participation.
Active female genital tract infection, requiring treatment per current CDC guidelines or symptomatic urinary tract infection (UTI). Infections requiring treatment include Chlamydia (CT), gonorrhea (GC), syphilis, active HSV lesions, chancroid, bacterial vaginosis, vaginal candidiasis, trichomonas, genital sores or ulcers, and, if clinically indicated, genital warts.
History of significant vaginal bleeding
Undiagnosed irregular uterine bleeding
Post-menopausal defined as 12 months of amenorrhea
Per participant report, abnormalities of the female genital tract, which, in the judgment of the investigator, might increase the risk of the study to the research participant.
Per participant report, history of cervical procedures (conization, Loop El electrosurgical Excision procedure (LEEP) procedure, cryosurgery) within the previous 6 months.
Per participant report, use of any vaginally administered medications within 4 weeks of enrollment
Per participant report, use of any vaginally administered products containing nonoxynol-9 (including condoms) or investigational products within 4 weeks of enrollment
Women who are pregnant or breastfeeding
Spermicide use within the last 30 days