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TerminatedNCT04901806Updated Mar 28, 2024

Study of PBI-200 in Subjects With NTRK-Fusion-Positive Solid Tumors

A Phase 1 interventional study of PBI-200 in Solid Tumor, Adult, Brain Tumor, Primary and Desmoplastic Small Round Cell Tumor, sponsored by Pyramid Biosciences. Terminated at 42 sites in 11 countries. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-03-28.

Sponsored by Pyramid Biosciences · Phase 1, Interventional, and Treatment

Why this study was terminated
Sponsor terminated development of PBI-200

From the registry’s dates

  • Primary completion was Jul 2023, 3 years 2 months ago, and no results have been posted to the registry.
Phase
Phase 1
Study type
Interventional
Enrollment
29
Allocation
Non-randomized
Ages
18 Years and older
Sex
All
01

Study summary

This is a first-in-human, open-label, multicenter, dose-escalation, safety, PK, and biomarker study of PBI-200 in subjects with NTRK-fusion-positive advanced or metastatic solid tumors.

Read the detailed description

This is a first-in-human, open-label, multicenter, dose-escalation, safety, PK, and biomarker study of PBI-200 in subjects with NTRK-fusion-positive advanced or metastatic solid tumors. Phase 1 will also include subjects with NTRK-amplified advanced or metastatic solid tumors or refractory EWSR1-WT1-fusion-positive desmoplastic small round cell tumors (DSRCTs).

Phase 1 is the dose-escalation portion of the study in which the evaluation of safety and tolerability and establishing the RP2D are primary objectives. Once the RP2D has been established, two expansion cohorts will open to accrual, a Non-Brain Primary Tumor cohort and a Primary Brian Tumor cohort.

Although this was intended to be a Phase 1/2 trial, the trial was terminated without proceeding to Phase 2.

02

Conditions studied

  • Solid Tumor, Adult
  • Brain Tumor, Primary
  • Desmoplastic Small Round Cell Tumor

Keywords

  • NTRK
  • NTRK Fusion
  • Resistance Mutation
03

In context

Neoplasms

9,365 studies on the registry are indexed under Neoplasms; 2,489 are open to participants now.

This study's enrollment of 29 is below the median of 50 across 7,253 interventional studies indexed under Neoplasms.

Browse Neoplasms studies →

Lead sponsor

Pyramid Biosciences is the lead sponsor of 7 studies on the registry; none are open to participants now.

Of its 7 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

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

Eligibility criteria

Key Inclusion Criteria:

  • Subject has one of the following solid tumors which has progressed on or following at least one systemic therapy regimen administered for advanced or metastatic disease or for which no approved therapy exists:

    • NTRK-fusion-positive, locally advanced (i.e., not amenable to surgical resection) or metastatic solid tumor Note: Subjects with any grade of malignant glioma previously treated with systemic therapy are eligible.

Phase 1

  • NTRK-gene amplified, locally advanced or metastatic solid tumor
  • EWSR1-WT1-positive DSRCTs.
  • Subjects with NTRK-fusion-positive solid tumors other than primary brain tumors must have previously received treatment with a TRK inhibitor, unless the subject does not have access to TRK-inhibitor therapy (e.g., no TRK inhibitor is marketed and available to the subject in the subject's country) or the subject has declined treatment with available marketed TRK inhibitors.
  • Subjects with NTRK-gene amplified solid tumors, primary brain tumors or EWSR1-WT1-positive DSRCTs may have received prior treatment with a TRK inhibitor but this is not required.

Phase 2

  • Has measurable disease by RECIST v1.1 for subjects with non-brain primary tumors or RANO criteria for subjects with primary brain tumors.
  • Subjects with non-brain primary tumors must have previously received treatment with a TRK inhibitor and a documented resistance mutation(s) (e.g., solvent front, gatekeeper or xDFG mutation). Archival tissue from a prior biopsy taken after the subject completed TRK inhibitor treatment but prior to additional systemic therapy may be used to meet this eligibility criterion with Medical Monitor approval.
  • Subjects with primary brain tumors may have received prior treatment with a TRK inhibitor but this is not required. Biopsies of brain tumors are not required for eligibility.

Key Exclusion Criteria:

  • Cytotoxic chemotherapy, biologic agent, investigational agent, or radiation therapy ≤ 3 weeks prior to the first dose of PBI-200 (6 weeks for nitrosoureas).

    • Subjects with either primary brain tumors or brain metastasis must have completed brain radiation therapy 12 weeks prior to the brain MRI obtained within 4 weeks of the first dose of PBI-200.
  • Small-molecule kinase inhibitors or hormonal agents ≤ 14 days and within 5 half-lives prior to the first dose of PBI-200.
05

Study design

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

Study arms

  • Experimental
    Phase 1 Dose Escalation

    Drug: PBI-200

  • Experimental
    Phase 2 Cohort Expansion

    Drug: PBI-200

Interventions

  • DrugPBI-200

    PBI-200 will be administered orally over continuous 28-day cycles

06

What researchers measure

Primary outcomes

  1. Phase 1: Number of patients with AEs

    Severity of AEs will be assessed according to the NCI CTCAE v5.0

    Time frame: Through study completion, estimated as an average of 36 months

  2. Phase 1: Recommended Phase 2 Dose

    Time frame: Approximately 12 months

  3. Phase 2: Cohort A - Overall Response Rate (ORR)

    Assessed using Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1

    Time frame: Through study completion, estimated as an average of 36 months

  4. Phase 2: Cohort B - ORR

    Assessed using Response Assessment in Neuro-Oncology (RANO) criteria

    Time frame: Through study completion, estimated as an average of 36 months

Secondary outcomes

  1. Phase 1: Area under the plasma drug concentration-time curve from 0 to 24 hours after one dose and after 28 doses

    Time frame: 29 days

  2. Phase 1: ORR

    Assessed by RECIST for subjects with non-brain primary tumors and by RANO for subjects with primary brain tumors

    Time frame: Through study completion, estimated as an average of 36 months

  3. Duration of Response (DoR)

    Assessed by RECIST for subjects with non-brain primary tumors and by RANO for subjects with primary brain tumors

    Time frame: Through study completion, estimated as an average of 36 months

  4. Progression-free Survival

    Assessed by RECIST for subjects with non-brain primary tumors and by RANO for subjects with primary brain tumors

    Time frame: Through study completion, estimated as an average of 36 months

07

Study locations

42 sites
  • John Wayne Cancer Institute at St. Johns Health Center
    Santa Monica, California 90404, United States
  • Stanford Hospital and Clinics
    Stanford, California 94305, United States
  • Sarah Cannon Research Institute at HealthONE
    Denver, Colorado 80218, United States
  • Florida Cancer Specialists
    Lake Mary, Florida 32746, United States
  • Sylvester Comprehensive Cancer Center (University of Miami)
    Miami, Florida 33136, United States
  • Miami Cancer Institute
    Miami, Florida 33176, United States
  • Dana-Farber Cancer Institute
    Boston, Massachusetts 02215, United States
  • Westchester Medical Center
    Hawthorne, New York 10532, United States
  • Thomas Jefferson University Hospital
    Philadelphia, Pennsylvania 19107, United States
  • Tennessee Oncology, PLLC
    Nashville, Tennessee 37203, United States
  • The University of Texas MD Anderson Cancer Center
    Houston, Texas 77030, United States
  • Peter MacCallum Cancer Centre
    Melbourne, Victoria 3000, Australia
  • Rigshospitalet, University Hospital of Copenhagen
    Copenhagen, 2100, Denmark
  • Institut Bergonie
    Bordeaux, 33076, France
  • Centre Léon Bérard
    Lyon, 69008, France
  • Hopital Europeen Georges Pompidou
    Paris, 75015, France
  • CHU Poitiers - Hopital la Miletrie
    Poitiers, 86000, France
  • Institut Gustave Roussy
    Villejuif, 94805, France
  • Dr. Senckenberg Institute of Neurooncology
    Frankfurt am Main, 60528, Germany
  • Universitaetsklinikum Heidelberg
    Heidelberg, 69120, Germany
  • Marienhospital Herne
    Herne, 44625, Germany
  • Queen Mary Hospital
    Pok Fu Lam, Hong Kong
  • Prince of Wales Hospital
    Sha Tin, Hong Kong
  • Azienda Ospedaliero Universitaria delle Marche
    Ancona, 60126, Italy
  • IRCCS Ospedale San Raffaele
    Milano, 20132, Italy
  • Fondazione IRCCS Istituto Nazionale Tumori
    Milano, 20133, Italy
  • IRCCS (IEO) Istituto Europeo di Oncologia
    Milano, 20141, Italy
  • IRCCS Istituto Nazionale Tumori Fondazione Pascale
    Napoli, 80131, Italy
  • Azienda Ospedaliera Universitaria Integrata Verona
    Verona, 37126, Italy
  • Seoul National University Bundang Hosptial
    Seongnam-si, Gyeonggi-do 13620, Korea, Republic of
  • The Catholic University of Korea St. Vincent Hosptial
    Suwon-si, Gyeonggi-do 16247, Korea, Republic of
  • Severance Hosptial, Yonsei University Health System
    Seoul, 03722, Korea, Republic of
  • Samsung Medical Center
    Seoul, 06351, Korea, Republic of
  • The Catholic University of Korea Soul St. Mary's Hosptial
    Seoul, 06591, Korea, Republic of
  • National Cancer Centre Singapore
    Singapore, 169610, Singapore
  • Hospital Universitari Vall d Hebron
    Barcelona, 08035, Spain
  • ICO l Hospitalet
    L'Hospitalet De Llobregat, 08908, Spain
  • Hospital Universitario Ramon y Cajal
    Madrid, 28034, Spain
  • Hospital Universitario La Paz
    Madrid, 28046, Spain
  • Hospital General de Catalunya
    Sant Cugat Del Vallès, 08195, Spain
  • The Christie
    Manchester, M20 4BX, United Kingdom
  • Royal Marsden Hospital Institute Cancer Research
    Sutton, SM2 5PT, United Kingdom
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 Mar 28, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04901806
Lead sponsor
Pyramid Biosciences
Responsible party
Sponsor
First posted
May 26, 2021
Start date
Jul 20, 2021
Primary completion
Jul 26, 2023
Completion
Jul 26, 2023
Last update
Mar 28, 2024

Study contacts

Chief Medical Officer
study director · Pyramid Biosciences

Oversight

Data monitoring committee
No
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 Mar 2024. You cannot join it, but the record below documents what was studied.

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