Recombinant Oncolytic Adenovirus 5 Encoding Non-secreting Interleukin-12 BioTTT001 clinical trials
How each study uses Recombinant Oncolytic Adenovirus 5 Encoding Non-secreting Interleukin-12 BioTTT001 is sorted by a rule, right about nine times in ten. Readers can ask us to read every study one by one.Ask us to read each study
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Approvals
The first approval found in each region, with its record
- United States
- Not in FDA's approval records
- European Union
- Not in EMA's list of EU-wide authorisations
From FDA's Drugs@FDA and Purple Book (through openFDA) and the European Medicines Agency, files of Sept 2026 and 27 Oct 2026. National approvals in Europe and other countries are not included. How this is worked out
How studies write it
Studies that test it under each name
Name
- BioTTT001 injection
- 4
Studies by the year they started
6 studies that test it; most in 2024 (3)
| Year | Studies |
|---|---|
| 2024 | 3 |
| 2025 | 2 |
| 2026 | 1 |
By phase
A phase 1/2 study counts in both.
What it is tested for
Each study’s main condition, where its own words name it, so a study counts once.
Who runs them
Industry 3 · Other 3
Beijing Bio-Targeting Therapeutics Technology Co., Ltd (3) · China Medical University, China (2) · Henan Cancer Hospital (1)
Coming up
From the study records. Dates are the sponsors’ own estimates and often move.
Reaching primary completion within a year · 2
Studies that test Recombinant Oncolytic Adenovirus 5 Encoding Non-secreting Interleukin-12 BioTTT001.
- Jul 2027Evaluating the Safety and Efficacy of BioTTT001 in Patients With Recurrent/Progressive High-grade Glioma.Phase 1/2 · Beijing Bio-Targeting Therapeutics Technology Co., Ltd
- Nov 2027A Clinical Study of BioTTT001 in Combination With SOX and Toripalimab in Patients With Gastric CancerPhase 2 · China Medical University, China
Studies
Open first, then newest update. How each study uses Recombinant Oncolytic Adenovirus 5 Encoding Non-secreting Interleukin-12 BioTTT001 is read from its arms, and is right about nine times in ten. Ask us to read each study. These are the studies that list it as an intervention; a search of ClinicalTrials.gov also finds studies that mention it only in a description, such as earlier treatment.
Testing it · 6
- Evaluating the Safety and Efficacy of BioTTT001 in Patients With Recurrent/Progressive High-grade Glioma.Enrolling by invitationPhase 1/2Beijing Bio-Targeting Therapeutics Technology Co., LtdNCT06763965Written as BioTTT001 injection
- A Clinical Study of BioTTT001 in Combination With Toripalimab and Regorafenib in Patients With Colorectal CancerNot yet recruitingPhase 1China Medical University, ChinaNCT06283134Written as BioTTT001 hepatic artery infusion
- Evaluate the Safety, Tolerability, Biodistribution Characteristics and Preliminary Efficacy of BioTTT001RecruitingPhase 1/2Henan Cancer HospitalNCT07264569Written as BioTTT001 injection
- A Clinical Study Evaluating the Safety and Efficacy of BioTTT001 in Patients With Malignant Solid TumorsEnrolling by invitationPhase 1Beijing Bio-Targeting Therapeutics Technology Co., LtdNCT06215846Written as BioTTT001 injection
- A Clinical Study of BioTTT001 in Combination With SOX and Toripalimab in Patients With Gastric CancerNot yet recruitingPhase 2China Medical University, ChinaNCT06283121Written as BioTTT001 intraperitoneal infusion
- A Clinical Study to Explore the Safety, Tolerability, and Efficacy of Recombinant Human nsIL12 Oncolytic Adenovirus Injection (BioTTT001) Combined With Neoadjuvant Treatment for Locally Advanced Breast CancerWithdrawnPhase 1Beijing Bio-Targeting Therapeutics Technology Co., LtdNCT07150767Written as BioTTT001 injection