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Open Label Immunotherapy of Myoma

Open Label Phase II Clinical Trial of Myoma Immunotherapy

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03550703
Acronym
V3-myoma
Enrollment
30
Registered
2018-06-08
Start date
2018-06-01
Completion date
2019-12-31
Last updated
2018-07-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Fibroid Uterus, Fibroma, Leiomyoma, Myoma;Uterus

Brief summary

Myoma of the uterus or uterine fibroids are benign tumors that appears in the myometrium or the muscular layer of the uterus. It is one of the most common diseases in pre-climax women, reaching 12-25% of all gynecological diseases. There is an opinion that the true prevalence of myoma is much larger and reaches up to 80%, i.e., practically every second woman has it, often without knowing about. For the treatment of MM, surgical removal of the nodes or removal of the uterus is used. In addition, GnRH-agonist therapy is practiced, as well as embolization to block blood flow in the tumor. We propose to evaluate the immunotherapy approach in an open label Phase II study in 20 women with myoma, for whom no alternative therapy is available.

Detailed description

Myoma or uterine fibroids are one of the most common gynecological diseases, which occurs in at least one third of women older than 35 years, and after 40 - in every second. We will test a new tablet preparation, V3-Myoma, obtained from hydrolyzed, inactivated blood and tumor tissues of patients with uterine myoma. When administered orally, V3-Myoma should cause a specific anti-tumor immune response and an anti-inflammatory effect. Such an effect is due to the phenomenon known in immunology, called oral tolerance, leading to a reduction in tumor mass and a decrease in inflammation. An important advantage of our approach is the absence of any negative side effects. In the next three month, we will conduct Phase II open label clinical study of this intervention in 30 women with confirmed diagnosis of myoma.

Interventions

BIOLOGICALV3-Myoma

Once daily oral pill of V3-Myoma

Sponsors

Immunitor LLC
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Masking description

no masking

Intervention model description

open label, single arm study

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

diagnosed myoma with single or multiple tumors presence of typical clinical symptoms associated with myoma -

Exclusion criteria

other gynecological diseases not related to myoma hysterectomy \-

Design outcomes

Primary

MeasureTime frameDescription
Change in tumor size compared to baselineOnce monthly for three monthsThis parameter will be evaluated by pelvic examination and transvaginal ultrasonography

Secondary

MeasureTime frameDescription
Changes in bleeding pattern at and between menstruationsDuring and between periods for three monthsSelf-evaluated by patient
Changes in level of pain associated with myoma, low back and legs, pelvic pressure and pain, if any3 monthsSelf evaluated by patient
Changes in frequent urination or difficulty in emptying the bladder or constipation3 monthsSelf evaluated by patient

Countries

Mongolia

Contacts

Primary ContactGalyna Kutsyna, MD, MD/PhD
kutsynagalyna@yahoo.com+97695130306
Backup ContactMarina Tarakanovskaya, MD
info@immunitor.com+97695130306

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026