ClinicalTrials.gg
RecruitingNCT06197568Updated Oct 19, 2026

Proof of Concept Study of Vaginal AZU-101 in Vulvovaginal Atrophy in Postmenopausal Women

A Phase 2 interventional study of Lasofoxifene Tartrate in Vulvo Vaginal Atrophy (VVA), sponsored by Azure Biotech Inc.. Recruiting at 1 site in United States. Open to female participants aged 45 Years to 60 Years. Per ClinicalTrials.gov, last updated 2026-10-19.

Sponsored by Azure Biotech Inc. · Phase 2, Interventional, and Treatment

From the registry’s dates

  • Started Jul 2026; still recruiting 4 months later.
Updated Oct 19, 2026Start date movedGo to Updates ↓
Phase
Phase 2
Study type
Interventional
Enrollment
90
Allocation
Randomized
Ages
45 Years to 60 Years
Sex
Female
01

Study summary

Study Objectives:

Primary:

  • To assess the safety, tolerability, and systemic pharmacokinetics (PK) of AZU-101

Secondary:

  • To evaluate efficacy of daily vaginal doses of AZU-101 in postmenopausal women on vaginal epithelium
Read the detailed description

This is a randomized, double-blind, placebo-controlled Phase 2A study of vaginal AZU-101 in healthy postmenopausal female participants with moderate to severe vulvovaginal atrophy (VVA) with no contraindications to selective estrogen receptor modulators (SERMs). AZU-101 is a vaginal formulation of lasofoxifene tartrate, a SERM that has high affinity to both estrogen receptor (ER) alpha (ERα) and ER beta (ERβ). This study plans to evaluate 3 doses of AZU-101 (1, 0.5, and 0.1μg) and placebo. Results of the first cohort (1μg AZU-101) will direct additional dosing cohorts (0.5 and 0.1μg AZU-101).

Safety and tolerability will be measured by vital signs, electrocardiogram (ECG) parameters, and the incidence of Treatment-Emergent Adverse Events (TEAEs) and concomitant treatments. The PK profile will be assessed using peak plasma concentration (Cmax), time to peak plasma concentration (tmax), and area-under-the-concentration-time-curve from time zero to infinity (AUC0-∞). Efficacy will be evaluated using vaginal pH, the vaginal Maturation Index (percentage of vaginal parabasal cells and superficial cells), and identification of the most bothersome symptom to the subject (dyspareunia, vaginal dryness, or vaginal irritation/itching).

Number of participants (planned): Up to approximately 90 healthy postmenopausal females, 45 to 60 years of age.

02

Conditions studied

  • Vulvo Vaginal Atrophy (VVA)

Browse trials for

Keywords

  • Dyspareunia
  • Vaginal atrophy
  • Postmenopausal symptoms
  • Vaginal dryness or irritation
  • Painful intercourse
03

In context

Dyspareunia

158 studies on the registry are indexed under Dyspareunia; 40 are open to participants now.

This study's planned enrollment of 90 is above the median of 63 across 126 interventional studies indexed under Dyspareunia.

Browse Dyspareunia studies →

Lead sponsor

This is the only study on the registry with Azure Biotech Inc. as lead sponsor.

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

04

Who can participate

Ages eligible
45 Years to 60 Years
Sexes eligible
Female
Accepts healthy volunteers
No

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

  1. 1. female participants between 45 and 60 years old, inclusive (at the time of signing ) with at least:

    1. 3 years of spontaneous amenorrhea; or
    2. At least 6 months postsurgical bilateral oophorectomy.
  2. Pain associated with sexual activity (dyspareunia)
  3. Vaginal pH ≥5.0
  4. Vaginal smear with the percentage of superficial cells less than 5%
  5. In the opinion of the Investigator, the participant will comply with the protocol and has a high probability of completing the study.
  6. Normal gynecological examination including Papanicolaou (Pap) smear (required for all participants, including those with prior hysterectomy)
  7. Good general health as evaluated by physical exam and lab assessments
  8. Agrees to not take any OTC medication, herbal product or nutritional supplement containing soy or plant extracts during the study conduct until final visit
  9. Agrees to not use any vaginal lubricants.
  10. If taking statin as a concomitant medication, must be on a stable dose for 3 months without plan to change during the course of the study and through study completion
  11. Agree to use a condom during sexual intercourse with a male partner during the study and for 1 month after the last dose.

Exclusion criteria

Exclusion Criteria:

  1. 1. Any to SERMs
  2. High risk for breast cancer and women with ductal carcinoma in situ (DCIS)
  3. A history of liver cancer
  4. A history of lung cancer
  5. Conditions resulting in an increased risk of hypercoagulability, including immobility and strong family history of hypercoagulability
  6. Documented coronary artery disease or at increased risk for major coronary events
  7. History of developing hypertriglyceridemia resulting from previous estrogen product treatment
  8. History of symptomatic cataracts
  9. History of endometrial polyps or abnormal endometrial findings on transvaginal ultrasound evaluation
  10. Use of any of the following:

    1. Oral estrogen-, progestin-, androgen-, or SERM-containing drug products within 3 months before Screening Visit
    2. Transdermal hormone products within 3 months before Screening Visit
    3. Vaginal hormone products (rings, creams, gels) within 3 months before Screening Visit
    4. Intrauterine progestins within 8 weeks before Screening Visit
    5. Progestin implants/injectables or estrogen pellets/injectables within 6 months before Screening Visit
    6. Any OTC medication, herbal product or nutritional supplement containing soy or plant extracts within 2 weeks prior to Screening Visit
  11. A history or active presence of medical disease that might confound the study or be detrimental to the participant, including but not limited to:

    1. Endometrial hyperplasia
    2. Undiagnosed vaginal bleeding
    3. History of a chronic liver or kidney dysfunction/disorder (e.g., or chronic renal failure)
    4. Thrombophlebitis, thrombosis, or thromboembolic disorders
    5. Cerebrovascular accident, stroke, or
    6. Myocardial infarction or ischemic heart disease
    7. or treatment for malignancy, within the previous 5 years, with the exception of basal cell carcinoma of the skin or squamous cell carcinoma of the skin
    8. History of estrogen dependent neoplasia, breast cancer, melanoma, or any gynecologic cancer, at any time
    9. Endocrine disease (except for controlled hypothyroidism or controlled non-insulin dependent diabetes mellitus)
    10. Known breast cancer gene (BRCA) mutation associated with increased risk of neoplasia
  12. TVUS of the endometrium at Screening with a double-wall thickness measurement greater than 5 mm
  13. A (BMI) \<18 and >34 kg/m2
  14. History of known alcohol or drug abuse within 1 year of the Screening Visit
  15. Positive urine drug or alcohol screen at Screening Visit
  16. Daily use of cigarettes or use of any electronic cigarettes
  17. Use of an drug or biologic within 60 days before administration of the first dose of study drug. Participants must agree not to participate in another research study of an investigational drug or device while enrolled in this study and for at least 30 days after completion of it.
  18. Any clinically important abnormalities on Screening physical examination, assessments, , or laboratory tests, including but not limited to:

    1. Unresolved cervical cytologic smear report of atypical glandular cells of undetermined significance (AGUS) or atypical squamous cells of undetermined significance (ASCUS). Cervical cytologic smear report of low-grade squamous intraepithelial lesion (SIL) or greater, cervical intraepithelial neoplasia (CIN) grade 1 or greater, or any reported dysplasia; Participants with ASCUS are eligible only if high risk human papilloma virus (HPV) result is negative.
    2. Unresolved findings suspicious for malignancy on the breast exam; incomplete mammogram result (Breast Imaging Reporting and Data System [BI-RADS] category 0) or unresolved findings suggestive of malignant changes or findings requiring short interval follow-up on the pre-study mammogram (participants must have mammography result of BI-RADS category 1 or 2 to enroll). Mammogram performed within 9 months prior to Screening Visit with documentation available may be used to evaluate study eligibility. The site must obtain a copy of the official report for the participant's study file, and it must be verified that the mammogram itself is available if needed for additional assessment.
    3. Hematocrit \<35% or >45%
    4. Serum creatinine >1.5 mg/dL.
    5. Serum (ALT) or serum aspartate aminotransferase (AST) >1.5 times the for the laboratory used
    6. Fasting total cholesterol >300 mg/dL (7.77 mmol/L) or triglycerides >300 mg/dL (3.39 mmol/L)
    7. Positive laboratory finding for Factor V Leiden mutation
    8. Fasting glucose >125 mg/dL
    9. Uncontrolled hypertension (participants with sitting BP >139 mmHg systolic or >89 mmHg diastolic) and may not be using more than 2 antihypertensive medications for the treatment of hypertension
    10. Hypotension; participants with sitting BP \<95 mmHg systolic or \<65 mmHg diastolic
    11. A clinically significant abnormal 12-lead ECG (e.g., showing previous myocardial infarction or other findings suggestive of ischemia)
    12. Positive (HIV), , hepatitis C, or active STD
    13. Untreated vaginal or urinary tract infection, or chronic urinary tract infections requiring repeated antibiotic treatment.
    14. Serum estradiol ≥20 pg/mL (≥73 pmol/L) at screening
    15. Thyroid-stimulating hormone (TSH) \<0.4 or >8.0 mIU/L
    16. History of lichen sclerosis vulvae
    17. Serum follicle-stimulating hormone (FSH) ≤30 IU/L
  19. Poor venous access
Terms in these criteria, in plain language(14)

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.

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.

Contraindication

A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.

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.

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.

TIA (transient ischaemic attack)

A “mini-stroke”: temporary stroke-like symptoms caused by reduced blood flow to part of the brain, spinal cord or eye, without signs of a new stroke on a scan.

Stroke symptoms need emergency care at once, even if they go away.

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.

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.

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.

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.

ALT and AST (liver enzymes)

Two enzymes measured in a routine blood test of the liver. Higher levels can mean the liver is under strain or damaged. SGPT and SGOT are older names for ALT and AST.

Criteria usually give a limit as a multiple of the upper limit of normal (ULN), often higher when cancer has spread to the liver.

ULN (upper limit of normal)

The top of the normal range for a blood test, as set by the laboratory that runs it. Each lab prints its own range next to your result.

“≤ 2.5 × ULN” means the result can be up to two and a half times that top value.

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.

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.

05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Triple (Participant, Care provider, Investigator)
Enrollment
90 participants (estimated)

Study arms

  • Experimental
    1 microgram dose lasofoxifene tartrate

    Vaginal administration 14 days

    Drug: Lasofoxifene Tartrate

  • Placebo comparator
    Placebo

    Placebo administered 14 days

    Drug: Lasofoxifene Tartrate

Interventions

  • DrugLasofoxifene Tartrate

    1.0 ug for 14 daily doses

    Also known as: AZU-101

06

What researchers measure

Primary outcomes

  1. Number of Participants Who Had Any Serious Adverse Events or Any Treatment Emergent Adverse Events With Severity Greater Than "Moderate" as measured by CTCAE v4.0

    Number of participants who had any serious adverse events or any adverse events with severity greater than "moderate," as determined by the Principal Investigator, using the composite safety assessment including clinical laboratory testing (full blood count, biochemistry, coagulation, lipid panel, thyroid hormone, urinalysis), ECG, vital signs, physical examination, transvaginal ultrasound, endometrial biopsy, and self-reporting of adverse events that are determined to be clinically significant.

    Time frame: 15 days

  2. Pharmacokinetics (AUC0-∞)

    Area under the concentration versus time curve in pg\*hr/mL

    Time frame: 24 hours after day 1 and day 14

  3. Pharmacokinetics (Tmax)

    Time to peak plasma concentration in hours

    Time frame: 24 hours after day 1 and day 14

  4. Pharmacokinetics (Cmax)

    Peak plasma concentration in pg/mL

    Time frame: 24 hours after day 1 and day 14

Secondary outcomes

  1. Efficacy (Vaginal pH)

    • Mean change from baseline in vaginal pH

    Time frame: Day 7 and 15

  2. Efficacy (Maturation index)

    * Mean change from baseline in percentage of superficial cells in the Maturation Index of the vaginal smear * Mean change from baseline in percentage of parabasal cells in the Maturation Index of the vaginal smear

    Time frame: Day 7 and 15

  3. Efficacy (symptoms)

    Mean change in the most bothersome symptom identified by the participant Efficacy outcome will be proportion of subjects who improve at least one grade

    Time frame: 15 days

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedDate before it movedWhere the date was before it moved

Started Jul 2026 (actual). Primary completion is estimated for Dec 2026, 5 months after the start.

Start moved once since we started tracking on Sep 25, 2026: Jun 2026 → Jul 2026, on Oct 19, 2026.

Earlier changes are on the record history on ClinicalTrials.gov ↗

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

Registered
Dec 5, 2023
First posted
Jan 9, 2024
StartActual
Jul 1, 2026was Jun 2026
Primary completionEst.
Dec 31, 2026
CompletionEst.
Jun 30, 2027
Last update
Oct 19, 2026
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.
Start date
Jun 1, 2026→Jul 1, 2026 (actual)
Oct 19, 2026
Site contacts
Changed at 1 site. See the sites
Show the site
  • Nucleus Network · Saint Paul, United StatesContact person changed (no phone or email listed)Contact person changed (no phone or email listed)
Oct 19, 2026
Show all 1 update
  1. Oct 19, 2026
    Start date Jun 1, 2026→Jul 1, 2026 (now actual)
    Site contacts Changed at 1 site. See the sites
    Show the site
    • Nucleus Network · Saint Paul, United StatesContact person changed (no phone or email listed)Contact person changed (no phone or email listed)
    + 1 other change: verification date

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT06197568
Lead sponsor
Azure Biotech Inc.
Collaborators
Nucleus Network Ltd
Responsible party
Sponsor
First posted
Jan 9, 2024
Start date
Jul 1, 2026
Primary completion
Dec 31, 2026 (estimated)
Completion
Jun 30, 2027 (estimated)
Last update
Oct 19, 2026

Study contacts

Howard Levy, MD PhD
Contact
hlevy@hlevyconsulting.com
(848) 992-5888
Susan L Levinson, PhD
Contact
slevinson@azurebiotech.com
973-4762430

Oversight

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

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

Contact study team

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion