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Priya Life Science Sponsor trial record
Sponsor · clinical trials

Beijing Pearl Biotechnology Limited Liability Company clinical trials

Source: ClinicalTrials.gov, U.S. National Library of Medicine — current trials in our China and USA registers with Beijing Pearl Biotechnology Limited Liability Company as lead sponsor. Synced 11 Nov 2026
4Current trials
2Recruiting now
7Drugs in these trials
2Trial registers
At a glance

Beijing Pearl Biotechnology Limited Liability Company is the lead sponsor of 4 current clinical trials in our China and USA registers. 2 are recruiting patients now. The most common phase is Phase 3. The drugs named most often in its trials are Vebreltinib, ANS014004 and Andamertinib. The most-studied condition is Non-Small Cell Lung Cancer.

ClinicalTrials.gov trials by status

  • Recruiting250%
  • Not yet open125%
  • Active, closed125%

Trials by phase

  • Phase 3250%
  • Phase 1/2125%
  • Phase 2/3125%
01

Clinical trials sponsored by Beijing Pearl Biotechnology Limited Liability Company

4 on ClinicalTrials.gov
StudyPhaseStatusStartRegisters
A Study of Vebreltinib and Platinum-Containing Double Agents in Subjects With MET-Positive
NCT06930794 · ClinicalTrials.gov ↗ · Non-Small Cell Lung Cancer
Phase 3 Recruiting 2025-07 China
A Confirmatory Clinical Study in NSCLC Patients With MET Exon 14 Mutation (KUNPENG-2)
NCT05989542 · ClinicalTrials.gov ↗ · Non-small Cell Lung Cancer
Phase 3 Recruiting 2023-10 China
A Study to Evaluate ANS014004 in Combination With EGFR-TKI in Non-Small Cell Lung Cancer
NCT07285148 · Non-Small Cell Lung Cancer, EGFR Mutation, Metastatic Lung Cancer
Phase 1/2 Not yet open 2026-06 USA
A Study of PLB1001 Enteric Capsules in the Treatment of sGBM/IDH Mutant Glioblastoma Patients With the ZM Fusion Gene (FUGEN).
NCT06105619 · ClinicalTrials.gov ↗ · Glioblastoma
Phase 2/3 Active, closed 2018-10 China

Registers list studies that are recruiting, about to open, active but closed to enrolment, or enrolling by invitation. The UK and USA registers cover industry-sponsored studies only. Titles and statuses are copied from the registry as published.

02

Drugs in Beijing Pearl Biotechnology Limited Liability Company trials

7 compounds

Drugs and biologicals named as interventions in these trials, with the number of this sponsor's trials that name each one. Placebos and generic comparators are excluded.

03

Conditions in Beijing Pearl Biotechnology Limited Liability Company trials

6 conditions
Non-Small Cell Lung Cancer2EGFR Mutation1Metastatic Lung Cancer1MET Alteration1Non-small Cell Lung Cancer1Glioblastoma1
04

By trial register

RegisterTrialsRecruiting
Clinical trials in China32
Clinical trials in USA10

A trial with sites in more than one country appears in each of those registers.

05

Other sponsors in Non-Small Cell Lung Cancer

SponsorTrials
AstraZeneca15
Sichuan Baili Pharmaceutical15
Merck Sharp & Dohme10
Hoffmann-La Roche6
Daiichi Sankyo6
Shanghai Chest Hospital5
Hunan Province Tumor Hospital4
Shanghai Pulmonary Hospital, Shanghai, China4
Regeneron Pharmaceuticals3
BioNTech3

Sponsors with the most current trials registered for this condition.

06

Questions about Beijing Pearl Biotechnology Limited Liability Company trials

How many clinical trials does Beijing Pearl Biotechnology Limited Liability Company sponsor?

Beijing Pearl Biotechnology Limited Liability Company is the lead sponsor of 4 current trials on ClinicalTrials.gov in our China and USA registers, as of the registry sync on 11 November 2026. Completed and withdrawn studies are not counted.

Are Beijing Pearl Biotechnology Limited Liability Company trials recruiting?

Yes. 2 of its 4 ClinicalTrials.gov trials are recruiting. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Which drugs is Beijing Pearl Biotechnology Limited Liability Company testing?

Its current trials name 7 drugs and biologicals as interventions. The most frequent are Vebreltinib (3), ANS014004 (1), Andamertinib (1), Cisplatin (1) and Etoposide (1). The number in brackets is how many of its trials name each drug.

Where does this information come from?

Every trial, status, phase and condition on this page is copied from public ClinicalTrials.gov and EU CTIS records by a daily sync, grouped by the sponsor name each registry records. It says nothing about the organisation beyond its registered trials, and it is not medical advice.

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How this page is built

Everything on this page is copied from public registry records — it is not written from memory, and nothing here describes the organisation beyond its registered trials. Each trial links to its own record so you can check it yourself.

This page is built automatically: a daily sync job reads the registry records behind our trial registers and groups every current trial by its lead sponsor name, ignoring legal-form suffixes such as Inc. or Ltd. A small, hand-checked list joins the same organisation's different registry names (for example its EU legal entity). There is no AI drafting and no per-sponsor editorial pass. The “last verified” date above is the timestamp of that sync, not a review date. Our general editorial approach is described in our editorial standards and corrections policy. The the registries data on this page was last retrieved on 11 Nov 2026. How every register is built: methodology · fixes we have made: corrections log.

Please verify before you rely on this. This page is general information for life-science and pharmaceutical professionals. It is not medical advice, and it has not been reviewed by a clinician — our editorial team holds life-science qualifications, not clinical ones. It is not exhaustive and may not reflect the most recent label change. Always check the official prescribing information (US Prescribing Information or EU SmPC) and speak to your doctor or pharmacist before acting on anything here. Drugs in the same class are not automatically interchangeable, and approvals, brand names and indications differ between the US, the EU/Ireland (EMA/HPRA) and other regions. Spotted an error? Tell us — we correct promptly and log it.