Nirogacestat in Patients With Kaposi Sarcoma

NCT07539454 | Not Yet Recruiting Phase 2 FDA Drug

• 3 other identifiers: AMC-118NCI-2026-00410UM1CA121947
• Study Type: interventional
• Target: 28
• Locations: 1 country
• Sites: 1

Brief Summary

This phase II trial studies how well nirogacestat works in treating patients with skin Kaposi sarcoma (KS). Several anti-cancer drugs work well in treating KS, but there is no treatment that cures KS. Nirogacestat binds to a protein called gamma secretase, which blocks the activation of other proteins called Notch receptors. Blocking these proteins may help keep tumor cells from growing and may kill them. Nirogacestat is a type of gamma secretase inhibitor. Nirogacestat may be effective in shrinking the size of KS lesions and reducing the spread of lesions.

Conditions

AIDS-Related Kaposi Sarcoma; Skin Kaposi Sarcoma

Outcome Measures

Primary Outcomes (1)

• Overall response rate (ORR)

  The ORR will be estimated for each dose group and for all groups combined. The 95% confidence intervals will be constructed for the ORR.

  Up to 5 years after completion of study treatment

Secondary Outcomes (5)

• Incidence of adverse events (AEs)

  Up to 5 years after completion of study treatment

• Duration of the response (DOR)

  From the first date on which a partial response or complete response is documented until progression or death due to any cause, assessed up to 5 years after completion of study treatment

• Cumulative proportion of study participants still in response

  At 1 year

• Blood biomarkers

  Up to 5 years after completion of study treatment

• Levels of Notch target and regulatory gene products

  Baseline up to 5 years after completion of study treatment

Other Outcomes (7)

• Tumor-associated Kaposi sarcoma-associated herpesvirus (KSHV) latent and lytic gene expression

  Up to 5 years after completion of study treatment

• Activation of Notch target genes and Notch regulatory genes

  Up to 5 years after completion of study treatment

• Tumor-associated endothelial-mesenchymal transition

  At the end of Cycle 1 (each cycle is 28 days)

Study Arms (1)

Treatment (nirogacestat)

EXPERIMENTAL

Patients receive nirogacestat PO BID on days 1-28 of each cycle. Cycles repeat every 28 days for 12 cycles in the absence of disease progression or unacceptable toxicity. Patients also undergo skin biopsy and chest X-ray during screening as well as blood sample collection throughout the study. Patients may also undergo an additional optional skin biopsy on study and CT throughout the study.

Procedure: Biospecimen Collection; Procedure: Chest Radiography; Procedure: Computed Tomography; Drug: Nirogacestat; Procedure: Skin Biopsy

Interventions

Biospecimen Collection PROCEDURE

Undergo collection of blood

Also known as: Biological Sample Collection, Biospecimen Collected, Specimen Collection

Treatment (nirogacestat)

Chest Radiography PROCEDURE

Undergo chest X-ray

Also known as: Chest X-ray

Treatment (nirogacestat)

Computed Tomography PROCEDURE

Undergo CT

Also known as: CAT, CAT Scan, Computed Axial Tomography, Computerized Axial Tomography, Computerized axial tomography (procedure), Computerized Tomography, Computerized Tomography (CT) scan, CT, CT Scan, Diagnostic CAT Scan, Diagnostic CAT Scan Service Type, tomography

Treatment (nirogacestat)

Nirogacestat DRUG

Given PO

Also known as: (S)-2-(((S)-6,8-Difluoro-1,2,3,4-tetrahydronaphthalen-2-yl)amino)-N-(1-(2-methyl-1-(neopentylamino)propan-2-yl)-1H-imidazol-4-yl)pentanamide, PF 03084014, PF-03084014, PF03084014

Treatment (nirogacestat)

Skin Biopsy PROCEDURE

Undergo skin biopsy

Also known as: Biopsy of Skin

Treatment (nirogacestat)

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Biopsy-proven KS involving skin with or without visceral involvement either newly diagnosed or refractory to or intolerant of one or more prior therapies.
• Patients must have cutaneous lesion(s) amenable to six total biopsies (minimum size of biopsy to be 4 mm), either six lesions \> 4 mm or one large lesion measuring 20 mm that can undergo serial biopsy, and at least five additional lesions measurable for assessment with no improvement over the past month.
• Hemoglobin ≥ 8 g/dL (within three months prior to study entry)
• Absolute neutrophil count (ANC) ≥ 1,000 cells/mm\^3 (within three months prior to study entry)
• Platelet count ≥ 100,000/mm\^3 (within three months prior to study entry)
• Calculated (method of Cockcroft-Gault) creatinine clearance (CrCl) ≥ 60 mL/min (within three months prior to study entry) (CrCl may also be obtained by the 24-hour collection method at the investigator's discretion)
• Total bilirubin should be ≤ 1.5x upper limit of normal (ULN) (within three months prior to study entry). If, however, the elevated bilirubin is felt to be secondary to atazanavir therapy, patients will be allowed to enroll on protocol if the total bilirubin is ≤ 3.5 mg/dL provided that the direct bilirubin is normal
• Aspartate aminotransferase (AST) (serum glutamic oxaloacetic transaminase \[SGOT\]) and alanine aminotransferase (ALT) (serum glutamic pyruvate transaminase \[SGPT\]) ≤ 3x ULN (within three months prior to study entry)
• Life expectancy ≥ 3 months.
• Ability and willingness to give informed consent.
• Females of childbearing potential (FCBP) must have a negative serum or urine pregnancy test defined as serum Estradiol (E2) \> 30 pg/mL, a serum follicle stimulating hormone (FSH) \< 40 mIU/L (measured on Day 3 in regularly menstruating females and age-matched), within 10-14 days prior and again within 24 hours of starting nirogacestat. FCBP must either commit to continued abstinence from heterosexual intercourse or the use of two acceptable methods of birth control, one highly effective method except oral contraceptives and one additional effective method at the same time , at the start of therapy to 7 days after discontinuation of nirogacestat, inclusive. Females and males of reproductive potential will be advised to use effective contraception during treatment with nirogacestat and for 7 days after the last dose. FCBP must also agree to ongoing pregnancy testing. Men must agree to use a latex condom during sexual contact with a FCBP even if they have had a successful vasectomy. All patients must be counseled at a minimum of every 28 days about pregnancy precautions and risks of fetal exposure. Patients must, in the opinion of the investigator, be capable of complying with the protocol.
• A female of childbearing potential is a sexually mature female who: 1) has not undergone a hysterectomy or bilateral oophorectomy; or 2) has not been naturally postmenopausal for at least 24 consecutive months (i.e., has had menses at any time in the preceding 24 consecutive months).
• All patients with HIV must be on antiretroviral therapy (ART) for HIV infection with CD4 count \> 50/mm\^3 and viral load \< 200 copies/mL. Patients must be on a stable regimen for at least 12 weeks prior to study entry. Patients may receive any Food and Drug Administration (FDA) approved ART except for zidovudine or protease inhibitors.
• There should be no evidence for improvement in KS in the 3 months prior to study entry for all participants, unless there is evidence for progression of KS in the 4 weeks immediately prior to study entry.
• If antiretroviral regimen contains zidovudine, efavirenz, etravirine, or protease inhibitors and viral load is suppressed (as measured by HIV viral load ≤ 200/mL), then ART must be adjusted to a less toxic therapy not containing these antivirals and enrollment may proceed without waiting 12 weeks. If on antiviral therapy with zidovudine, efavirenz, etravirine, or protease inhibitors, and viral load is not suppressed (as measured by HIV viral load ≥ 200/mL), then ART must be adjusted to a less toxic regimen allowing for optimal viral suppression and must demonstrate stability for at least 12 weeks prior to study entry.

You may not qualify if:

• Concurrent, acute, active opportunistic infection other than oral thrush or genital herpes within 14 days of enrollment.
• Patients for whom front-line cytotoxic therapy is indicated (i.e., symptomatic visceral or pulmonary KS or symptomatic KS impairing functional status).
• Concurrent neoplasia requiring cytotoxic therapy.
• Anti-neoplastic treatment for KS (including chemotherapy, radiation therapy, local therapy including topical 5-FU, biological therapy, or investigational therapy) within four weeks of study entry.
• Any ongoing glucocorticoid treatment (within last three months, lasting longer than 14 days) except for that required for replacement therapy in adrenal insufficiency or inhaled glucocorticoids for the treatment of asthma.
• Any steroid treatment with equivalent of more than 10 mg prednisone/day lasting longer than 14 days in the last 3 months.
• Patient is ≤ 2 years free of another primary malignancy. Exceptions include the following:
• Basal cell skin cancer.
• Cervical carcinoma in situ.
• Anal carcinoma in situ.
• Previous local therapy of any KS-indicator lesion unless the lesion has clearly progressed since treatment. Any prior local treatment to indicator lesions regardless of the elapsed time should not be allowed unless there is evidence of clear-cut progression of said lesion.
• Use of any investigational drug or treatment within four weeks prior to enrollment.
• Physical or psychiatric conditions that in the estimation of the investigator place the patient at high risk of toxicity or non-compliance.
• Female patients who are pregnant, lactating, or breast-feeding.
• Patients requiring blood transfusions to maintain hemoglobin eligibility.

Sponsors & Collaborators

• AIDS Malignancy Consortium: lead
• National Cancer Institute (NCI): collaborator

Study Sites (1)

Siteman Cancer Center at Washington University

St Louis, Missouri, 63110, United States

Location

MeSH Terms

Conditions

AIDS-related Kaposi sarcoma

Interventions

Specimen Handling; X-Rays; nirogacestat

Intervention Hierarchy (Ancestors)

Clinical Laboratory Techniques; Diagnostic Techniques and Procedures; Diagnosis; Investigative Techniques; Electromagnetic Radiation; Electromagnetic Phenomena; Magnetic Phenomena; Physical Phenomena; Radiation; Radiation, Ionizing

Study Officials

• Lee Ratner

  AIDS Malignancy Consortium

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: NETWORK
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: April 6, 2026
• First Posted: April 20, 2026
• Study Start (Estimated): September 17, 2026
• Primary Completion (Estimated): February 17, 2030
• Study Completion (Estimated): February 17, 2030
• Last Updated: April 20, 2026

Record last verified: 2026-04

Locations

US (1)