ClinicalTrials.gg
TerminatedNCT04249947Updated Feb 17, 2025

P-PSMA-101 CAR-T Cells in the Treatment of Subjects With Metastatic Castration-Resistant Prostate Cancer (mCRPC) and Advanced Salivary Gland Cancers (SGC)

A Phase 1 interventional study of P-PSMA-101 CAR-T cells and Rimiducid in Prostatic Neoplasms, Castration-Resistant, Neoplasms by Histologic Type and Neoplasms, Prostate, sponsored by Poseida Therapeutics, Inc.. Terminated at 10 sites in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-02-17.

Sponsored by Poseida Therapeutics, Inc. (part of Hoffmann-La Roche) · Phase 1, Interventional, and Treatment

Why this study was terminated
Study closed

From the registry’s dates

  • Primary completion was Sep 2024, 2 years 1 month ago, and no results have been posted to the registry.
Phase
Phase 1
Study type
Interventional
Enrollment
40
Allocation
Non-randomized
Ages
18 Years and older
Sex
All
01

Study summary

An open-label, multi-center, single and cyclic ascending dose study of P-PSMA-101 autologous CAR-T cells in patients with mCRPC and SGC.

Read the detailed description

This is an open label, multi-center Phase 1 study that will follow a 3 + 3 design of dose-escalating cohorts of single and multiple doses of P-PSMA-101 to determine a Recommended Phase 2 Dose (RP2D). Additional participants will be treated with P-PSMA-101 at the determined RP2D.

Following consent, enrolled participants will undergo a leukapheresis procedure to obtain peripheral blood mononuclear cells (PBMCs) which will be sent to a manufacturing site to produce P-PSMA-101 CAR-T cells. The cells will then be returned to the investigational site and administered after a lymphodepleting chemotherapy regimen. Rimiducid may be administered as indicated.

02

Conditions studied

  • Prostatic Neoplasms, Castration-Resistant
  • Neoplasms by Histologic Type
  • Neoplasms, Prostate
  • Prostate Cancer
  • Metastatic Castration-resistant Prostate Cancer
  • Neoplasms
  • Prostatic Neoplasms
  • Genital Neoplasms, Male
  • Urogenital Neoplasms
  • Neoplasms by Site
  • Prostatic Disease
  • Salivary Gland Cancer
  • Salivary Gland Tumor
  • Adenoid Cystic Carcinoma
  • Salivary Duct Carcinoma
  • Mucoepidermoid Carcinoma
  • Acinic Cell Tumor

Keywords

  • CAR-T cells
  • metastatic castration-resistant prostate cancer (mCRPC)
03

In context

Prostatic Neoplasms, Castration-Resistant

85 studies on the registry are indexed under Prostatic Neoplasms, Castration-Resistant; 28 are open to participants now.

This study's enrollment of 40 is below the median of 82 across 62 interventional studies indexed under Prostatic Neoplasms, Castration-Resistant.

Browse Prostatic Neoplasms, Castration-Resistant studies →

Lead sponsor

Poseida Therapeutics, Inc. is the lead sponsor of 6 studies on the registry; none are open to participants now.

First submitted before Poseida Therapeutics, Inc. became part of Hoffmann-La Roche.

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

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
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

  • Subjects ≥18 years of age
  • Must have a confirmed diagnosis of mCRPC or SGC
  • Must have by 1.1 or bone only with measurable PSA (≥1 ng/mL) (mCRPC subjects only)
  • Must have progressed by PCWG3 and/or RECIST 1.1 (mCRPC subjects only)
  • Must be willing to practice from screening and for 2 years after the last administration of P-PSMA-101
  • Must have adequate vital organ function within pre-determined parameters
  • Must have an (ECOG) performance status of 0 to 1

Exclusion criteria

Exclusion Criteria:

  • Has inadequate venous access and/or to leukapheresis
  • Has an active second in addition to mCRPC or SGC, excluding low-risk neoplasms such as non- basal cell or squamous cell skin carcinoma
  • Has a history of or active disease
  • Has a history of significant central nervous system (CNS) disease, such as stroke or epilepsy
  • Has an active systemic (viral, bacterial or fungal) infection
  • Has received anti-cancer medications (excluding GnRH targeted therapies) within 2 weeks of the time of initiating conditioning chemotherapy
  • Has received medications (including anti-cancer medications) within 2 weeks of initiating leukapheresis and/or expected to require them while enrolled in the study
  • Has received systemic therapy within 2 weeks of either the required leukapheresis or is expected to require it during the course of the study
  • Has or symptomatic CNS involvement
  • Has a history of significant ocular disease
  • Has a history of significant liver disease or active liver disease
  • Has liver metastases (\<5 lesions and maximum diameter \</= 2.5 cm permitted)
  • Has a history of or known predisposition to HLH or MAS
Terms in these criteria, in plain language(11)

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.

Measurable disease

The amount of disease can be tracked with a defined measurement, so the study can see whether it shrinks or grows. It might be a tumour measured on a scan or, in some blood cancers such as myeloma, a marker measured in blood or urine.

The criteria or the study team say which measurement counts — having no tumour visible on a scan does not by itself rule you out.

RECIST

The standard rules for measuring tumours on CT or MRI scans, to tell whether a cancer is shrinking, stable or growing during treatment.

“Measurable disease per RECIST 1.1” usually means at least one tumour 10 mm or more at its longest on a CT scan, or a lymph node 15 mm or more across its short axis.

Metastases

Cancer that has spread from where it began to other parts of the body. “Metastatic” cancer is cancer that has spread this way.

Contraception

Ways of preventing pregnancy. “Highly effective” methods fail less than 1% of the time a year when used correctly — for example an IUD or an implant.

Criteria usually say which methods count and how long to keep using them after the last dose, sometimes for male participants too. Some studies accept a partner’s vasectomy if it was confirmed successful and that person is the participant’s only sexual partner.

ECOG performance status

A scale of how much an illness limits everyday activity. For people being assessed to join a study, scores run from 0 (fully active) to 4; lower is more active.

0
Fully active, no restrictions.
1
Limited in strenuous activity, but walking and able to do light work, such as housework or office work.
2
Walking and able to look after yourself, but unable to work; up and about more than half of waking hours.
3
Able to look after yourself only in part; in bed or a chair more than half of waking hours.
4
Unable to look after yourself at all; in bed or a chair all day.

Studies most often ask for 0–1 or 0–2. Your doctor gives the score; the WHO scale uses the same steps. The full scale also has 5, which records death.

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.

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.

Autoimmune disease

A condition in which the immune system attacks the body’s own tissues, such as rheumatoid arthritis, lupus, psoriasis, type 1 diabetes or inflammatory bowel disease.

Immunotherapy studies often leave out active autoimmune disease, and some name exceptions, such as thyroid disease on replacement hormone. Check the exceptions this study lists.

Immunosuppression

A weakened immune system. It can come from an illness, such as HIV or some blood cancers, or from medicines that turn the immune system down, for example after an organ transplant or for an autoimmune disease; steroids at higher doses count.

Read whether the line is about a condition or about medicines, and which medicines and doses it means.

Corticosteroids (steroids)

Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.

Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.

Brain metastases

Cancer deposits in the brain from a cancer that started elsewhere in the body (CNS metastases include the spinal cord).

Studies differ: some leave out any brain metastases, some accept ones treated and stable for some weeks. Check what this study allows.

05

Study design

Phase
Phase 1
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Sequential assignment
Masking
None (open label)
Enrollment
40 participants (actual)

Study arms

  • Experimental
    P-PSMA-101 CAR-T cells (Single Dose - Part 1a)

    Single ascending dose cohorts, given in a single intravenous infusion of CAR-T cells, following conditioning chemotherapy regimen A. Rimiducid may be administered as indicated.

    Biological: P-PSMA-101 CAR-T cells · Drug: Rimiducid

  • Experimental
    P-PSMA-101 CAR-T cells (Multiple Dose - Part 1b)

    Cyclic administration of ascending dose cohorts, given in a single intravenous infusion of CAR-T cells, following conditioning chemotherapy regimen A. Rimiducid may be administered as indicated.

    Biological: P-PSMA-101 CAR-T cells · Drug: Rimiducid

  • Experimental
    P-PSMA-101 CAR-T cells (Single Dose - Part 1c)

    Single ascending dose cohorts, given in a single intravenous infusion of CAR-T cells, following conditioning chemotherapy regimen B. Rimiducid may be administered as indicated.

    Biological: P-PSMA-101 CAR-T cells · Drug: Rimiducid

  • Experimental
    P-PSMA-101 CAR-T cells (Multiple Dose - Part 1d)

    Cyclic administration of ascending dose cohorts, given via intravenous infusions of CAR-T cells, following conditioning chemotherapy regimen B. Rimiducid may be administered as indicated.

    Biological: P-PSMA-101 CAR-T cells · Drug: Rimiducid

Interventions

  • BiologicalP-PSMA-101 CAR-T cells

    P-PSMA-101 is an autologous chimeric antigen receptor (CAR) T-cell therapy designed to target prostate cancer cells expressing the cell surface antigen prostate-specific membrane antigen (PSMA).

  • Rimiducid (safety switch activator) may be administered as indicated

06

What researchers measure

Primary outcomes

  1. Assess the Safety of P-PSMA-101

    Incidence and severity of treatment-emergent adverse events

    Time frame: Baseline through 15 years

  2. Determine the maximum tolerated dose of P-PSMA-101

    Rate of dose limiting toxicities (DLT)

    Time frame: Baseline through Day 28

  3. Assess the efficacy of P-PSMA-101 (ORR)

    According to the Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1, secondarily Immune Response Evaluation Criteria in Solid Tumors (iRECIST), and Prostate Cancer Response assessed by Prostate Cancer Working Group 3 (PCWG3) criteria: Overall Response Rate (ORR)-Percentage of patients with complete response (CR) or partial response (PR).

    Time frame: Baseline through 15 years

07

Study locations

10 sites
  • City of Hope Comprehensive Cancer Center
    Duarte, California 91010, United States
  • University of California San Diego
    San Diego, California 92093, United States
  • University of California San Francisco
    San Francisco, California 94143, United States
  • Sarah Cannon Research Institute at HealthONE
    Denver, Colorado 80218, United States
  • Tulane University Hospital and Clinic
    New Orleans, Louisiana 70112, United States
  • University of Maryland, Baltimore
    Baltimore, Maryland 21201, United States
  • Dana-Farber Cancer Institute
    Boston, Massachusetts 02215, United States
  • Massachusetts General Hospital
    Boston, Massachusetts 02215, United States
  • Memorial Sloan Kettering Cancer Center
    New York, New York 10065, United States
  • Tennessee Oncology
    Nashville, Tennessee 37203, United States
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 17, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04249947
Responsible party
Sponsor
First posted
Jan 31, 2020
Start date
Feb 28, 2020
Primary completion
Sep 30, 2024
Completion
Sep 30, 2024
Last update
Feb 17, 2025

Study contacts

Rajesh Belani, M.D.
study director · Sponsor Executive Medical Director

Oversight

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

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This study is terminated, as verified in Jan 2025. You cannot join it, but the record below documents what was studied.

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