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Organization (Industry)

TELIX PHARMACEUTICALS LIMITED

ClinicalTrials.gov lists TELIX PHARMACEUTICALS LIMITED as lead sponsor of 24 trials, counting the companies grouped under it. TELIX PHARMACEUTICALS LIMITED itself has 17 active development programs and 4 approved assets.

AU Industry Manufacturer CIK 0002007191
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7 0 2018 2026

Trials started per year with this organization as sponsor or collaborator, 1990 onward. Companies grouped under this one are not included. The series also counts trials where the organization is a collaborator; the lead-sponsor trial count does not.

2026 is partial: 3 registered with a 2026 start date. The dashed outline is the pace from the 2 registered with a start date through September, planned starts included, not adjusted; not a forecast. No forecast is made for this organization: it averages 4.4 trial starts a year over the five years to September, under the 5 a year the method needs.

This page covers TELIX PHARMACEUTICALS LIMITED and 2 companies grouped under it: 24 lead-sponsored trials (23 its own, 1 in the grouped companies) and 4 legal-entity registrations (4 its own, 0 in the grouped companies).

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Companies grouped under this page (2)

Shown in this order: most lead trials first.

Companies grouped under this page
Company Lead trials Legal entities
QSAM Therapeutics, Inc. 1 0
Telix Innovations S.A. 0 0

Disease areas (32)

Shown in this order: most trials first.

Disease areas
Disease area Trials
Prostatic Neoplasms 11
Carcinoma, Renal Cell 10
Kidney Neoplasms 10
Glioma 6
Glioblastoma 4

Trials by start year as sponsor or collaborator (9)

Shown in this order: most recent first. 2026 is partial: trials registered with a 2026 start date so far, not a full year.

Show the table of trials by start year as sponsor or collaborator
Trials by start year as sponsor or collaborator
Year Trials started
2026 (partial year) 3
2025 5
2024 5
2023 7
2022 3
2021 3
2020 2
2019 3
2018 1

Prediction, not a registry value: median of 35 months from start to primary completion across 8 trials still running at the 2026-10-09 snapshot; registered median of 20 months across 11 trials with a primary completion typed Actual. Source: ClinicalTrials.gov / AACT (CTTI), public domain.

Active development programs (17)

Shown in this order: max phase, then active trials.

Active development programs
Drug Disease area Max phase Trials
68Ga-PSMA-11 Prostatic Neoplasms Phase 3 2
DOCETAXEL Prostatic Neoplasms Phase 3 1
89Zr-TLX250 PET/CT Carcinoma, Renal Cell Phase 3 1
89Zr-TLX250 PET/CT Kidney Neoplasms Phase 3 1
177Lu-TLX591 Prostatic Neoplasms Phase 3 1

Approved assets (4)

Shown in this order: max phase first.

Approved assets
Drug Trials
68Ga-PSMA-11 2
DOCETAXEL 1
Enzalutamide 1
Abiraterone 1

Sponsor delivery record (1)

Enrollment hit target: the share of this sponsor's lead-sponsored trials whose actual enrollment reached the planned enrollment. On time: the share whose actual primary completion date was no later than the planned date. Each share counts only trials where we observed an estimated figure before the actual one, and n is that number of trials. Below 5 trials the count is shown as a fraction, not a percentage.

Sponsor delivery record
Enrollment Timeline
18% hit target (n=11) 36% on time (n=11)

Journals published in (21)

Shown in this order: most published in first.

Journals published in
Journal Publications
Journal of nuclear medicine : official publication, Society of Nuclear Medicine 10
Clinical cancer research : an official journal of the American Association for Cancer Research 4
European urology 4
EJNMMI research 3
European journal of nuclear medicine and molecular imaging 3

US granted patents (1)

Patents are not classified by disease area in the source, so this is the organization's overall portfolio, not a split by disease.

US granted patents
US patents granted Granted in the last 5 years Most recent grant
1 1 2025-08-12

SEC-reported annual financials (4)

Shown in this order: newest fiscal year first; SEC EDGAR XBRL companyfacts, USD as reported.

SEC-reported annual financials
Fiscal year Revenue (USD) Net income (USD) R&D (USD)
2025 803,794,000 -7,125,000 171,249,000
2024 516,551,000 33,685,000 127,930,000
2023 332,978,000 4,208,000 85,315,000
2022 not reported not reported not reported

Financing and grant events (10)

Shown in this order: most recent first.

Financing and grant events
Date Round type Amount (USD) Source
2026-04-23 Debt financing 600,000,000 Sec extracted
2026-04-20 Other financing not disclosed Sec extracted
2026-04-14 Debt financing not disclosed Sec extracted
2026-04-14 Debt financing not disclosed Sec extracted
2026-04-13 Royalty / licensing not disclosed Sec extracted

Climate targets, as filed (1)

Climate targets, as filed
Reporting year Net-zero target
2025 not disclosed

Workforce and board diversity, as filed (1)

Workforce and board diversity, as filed
Reporting year Workforce % women Board % women
2025 not disclosed not disclosed

Organization relationships (8)

Shown in this order: most evidence first.

Organization relationships
Related organization Relationship Evidence
Medpace Holdings, Inc. Uses vendor 1
UCLA Health Co sponsors trial with 1
Government of the United States of America Co sponsors trial with 1
Mass General Brigham Co sponsors trial with 1
Radboud University Medical Center Co sponsors trial with 1

Latest dated events (44)

Shown in this order: newest first.

Latest dated events
Date Event Source
2026-10 Trial started Clinical trials (ClinicalTrials.gov) (ClinicalTrials.gov, U.S. National Library of Medicine; AACT database, Clinical Trials Transformation Initiative (CTTI))
2026-09-16 Trial started Clinical trials (ClinicalTrials.gov) (ClinicalTrials.gov, U.S. National Library of Medicine; AACT database, Clinical Trials Transformation Initiative (CTTI))
2026-09-11 PDUFA decision date Regulatory decision dates extracted from SEC filings
2026-04-23 Debt facility Funding rounds and grants (NIH RePORTER + SEC EDGAR)
2026-04-20 Financing Funding rounds and grants (NIH RePORTER + SEC EDGAR)

Biomarker capability evidence (95)

Shown in this order: tier desc, then gene symbol.

Biomarker capability evidence
Gene Role Evidence
ALB Trial sponsor Named in trial inclusion criteria
CSF2 Trial sponsor Named in trial inclusion criteria
CSF3 Trial sponsor Named in trial inclusion criteria
DPEP1 Trial collaborator Named in trial inclusion criteria
FOLH1 Trial sponsor Named in trial inclusion criteria

Not on this page

Checked, with nothing recorded for this organization: related companies not grouped here, fda warning letters, fda untitled letters, fda inspection record, fda recalls, fda import refusals, manufacturing and distribution sites, clia clinical laboratory certificates, and biomarkers this organization publishes on.