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Clinical trial updates
Drug and device trials that companies register on ClinicalTrials.gov: newly completed phase 3 studies, changes of status and the dates a study is due to finish.
About this data
- What it is
- ClinicalTrials.gov is the US registry of clinical studies. Drug and device makers register their trials there and update the record as each study moves on. We list the studies that companies sponsor, and match the sponsor to a public company when the name lines up. The page opens on Phase 3 studies marked completed, the late-stage trials that come before a request for approval. Change View to see the changes of status we have noticed, or every recent update.
- Who files it
- The sponsor of the study, in its record on ClinicalTrials.gov. The registry is run by the US National Library of Medicine and does not check what sponsors report.
- How current
- We check the registry every day. Sponsors update records on their own schedule, from the same week to months later, so a change can appear in the registry well after it happened.
- Terms
- ClinicalTrials.govClinicalTrials.gov is the US government's registry of clinical studies, run by the National Library of Medicine. Sponsors register a study before it starts and update the record as it goes. The registry does not check what a sponsor reports.Phase 3The late stage of testing, usually with hundreds or thousands of people, to confirm that a treatment works and to find side effects. A study marked Phase 2/3 covers both stages.statusThe registry's own word for where a study stands: not yet recruiting, recruiting, active but not recruiting, completed, terminated (stopped early), withdrawn (never started), suspended, or unknown (the sponsor has not confirmed the record for a long time).completedThe sponsor has marked the study as finished. It says nothing about whether the treatment worked: results, if any, are reported separately and often later.status changesOur history of status changes starts the day we first stored each study, so a change made before that is not shown. The date is when we noticed the change, which can be later than when the sponsor made it.primary completionThe date the last participant is examined for the main question the study asks. The study can run on after it, for follow-up. Sponsors enter the date and revise it, and an estimated date can pass without an update.company matchWe match the sponsor's name to a public company automatically, and by hand for the large drugmakers. A subsidiary or a differently spelled name can be missed, so a study with no ticker does not mean the sponsor is private.
- Worth knowing
- A completed study is not a result: the registry says the study ended, not whether the treatment worked. Status changes start on the day we first stored each study, so earlier changes are not shown. Dates are the sponsor's own, and an estimated date can pass without an update. We match sponsors to companies automatically, with a hand-checked list for the large drugmakers, so a study with no ticker may still belong to a public company. This is information about studies, not a forecast of what they will show or of a stock's price.
- Not to be confused with
- FDA approvals and clearances: what the FDA decided, not what a sponsor reports about a study.
All of this comes from ClinicalTrials.gov, the US registry of clinical studies. We are not affiliated with it.
Source and freshness · Information, not investment advice (disclaimer).
Studies updated per day, last 30 days
All industry-sponsored studies Sponsor matched to a public company
By the day the sponsor last updated the study's record. A study updated twice counts once, on its latest day.
Latest clinical trial updates
Showing: ticker ALLR · All recent updates
Studies by the date their record was last updated.
| Updated | Study | SponsorWe match the sponsor's name to a public company automatically, and by hand for the large drugmakers. A subsidiary or a differently spelled name can be missed, so a study with no ticker does not mean the sponsor is private. | PhaseThe late stage of testing, usually with hundreds or thousands of people, to confirm that a treatment works and to find side effects. A study marked Phase 2/3 covers both stages. | StatusThe registry's own word for where a study stands: not yet recruiting, recruiting, active but not recruiting, completed, terminated (stopped early), withdrawn (never started), suspended, or unknown (the sponsor has not confirmed the record for a long time). | Enrolled | Primary completionThe date the last participant is examined for the main question the study asks. The study can run on after it, for follow-up. Sponsors enter the date and revise it, and an estimated date can pass without an update. | Source |
|---|---|---|---|---|---|---|---|
| Jul 30, 2026 | Clinical Pre-screening Protocol for Ovarian Cancer NCT03877796 · Ovarian Cancer Drug Response Predictor® (DRP) | ALLR Allarity Therapeutics | — | Recruiting | 60 | Jun 2027 | Registry ↗ |
| Jun 1, 2026 | Study of PARPi 2X-121 as Monotherapy and in Combination With Dovitinib in Patients With Advanced So… NCT05571969 · Advanced Solid Tumors 2X-121 600 mg, 2X-121 800 mg | ALLR Allarity Therapeutics | Phase 1 | Terminated | 14 | Feb 19, 2024 | Registry ↗ |
| Mar 12, 2026 | Anti-tumor Effect of Ixabepilone in Metastatic Breast Cancer (mBC) Selected by the Ixabepilone DRP. NCT04796324 · Metastatic Breast Cancer Ixabepilone Injection | ALLR Allarity Therapeutics | Phase 2 | Terminated | 13 | Dec 1, 2024 | Registry ↗ |
| Aug 28, 2025 | Investigation of the Anti-tumor Effect of 2X-121 in Patients With Recurrent, Advanced Ovarian Cancer NCT03878849 · Advanced Ovarian Cancer 2X-121, 2X-121 | ALLR Allarity Therapeutics | Phase 2 | Recruiting | 40 | Mar 2027 | Registry ↗ |
| Jan 23, 2025 | Irofulven in AR-targeted and Docetaxel-Pretreated mCRPC Patients With Drug Response Predictor (DRP®) NCT03643107 · Metastatic Castration-Resistant Prostate Cancer Patients Irofulven, Prednisolone 10 mg | ALLR Allarity Therapeutics | Phase 2 | Completed | 15 | Oct 1, 2021 | Registry ↗ |
| Jan 23, 2025 | Investigation of Anti-tumour Effect and Tolerability of the PARP Inhibitor 2X-121 in Patients With… NCT03562832 · Metastatic Breast Cancer PARP inhibitor 2X-121 | ALLR Allarity Therapeutics | Phase 2 | Completed | 20 | Apr 1, 2024 | Registry ↗ |
| Feb 24, 2022 | Phase I/II Study to Evaluate the Safety and Tolerability of LiPlaCis in Patients With Advanced or R… NCT01861496 · Phase 1: Advanced or Refractory Solid Tumours, Phase 2 Part… LiPlaCis | ALLR Allarity Therapeutics | Phase 1/2 | Completed | 50 | Oct 2021 | Registry ↗ |
| Jan 30, 2020 | Safety and Pharmacokinetics of Rising Doses of APO010 in Relapsed/Refractory Multiple Myeloma Patie… NCT03196947 · Relapsed/Refractory Multiple Myeloma APO010 | ALLR Allarity Therapeutics | Phase 1/2 | Terminated | 1 | Jan 16, 2020 | Registry ↗ |
8 items, most recent first (up to 50). Each row links to the study's page on ClinicalTrials.gov. Updated Nov 15, 2026, 6:44 PM EST.
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