Last reviewed · How we verify

NCT04886622

A Study of DT2216 in Relapsed/Refractory Malignancies

Completed Phase 1 Last updated 16 April 2025
What this trial tests

Phase 1 trial testing DT2216 in Solid Tumor in 20 participants. Completed in 30 June 2024.

Timeline
25 August 2021
Primary endpoint
30 June 2024
30 June 2024

Quick facts

Lead sponsorDialectic Therapeutics, Inc
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsequential
Maskingnone
Primary purposetreatment
Enrollment20
Start date25 August 2021
Primary completion30 June 2024
Estimated completion30 June 2024
Sites3 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Dialectic Therapeutics, Inc — full company profile →

Who can join

18 and older, any sex, with Solid Tumor or Hematologic Malignancy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

A Phase 1, Open-Label, Dose Escalation, and Cohort Expansion Study to Evaluate the Safety, Tolerability, Pharmacokinetics (PK) and Clinical Activity of DT2216, an Antiapoptotic Protein Targeted Degradation Compound, in Subjects with Relapsed or Refractory Malignancies

Publications & conference data

8 peer-reviewed publications reference this trial (live from Europe PMC):

  1. PROTAC targeted protein degraders: the past is prologue.
    Békés M, Langley DR, Crews CM. · · 2022 · cited 2098× · PMID 35042991 · DOI 10.1038/s41573-021-00371-6
  2. Recent advances in targeting the "undruggable" proteins: from drug discovery to clinical trials.
    Xie X, Yu T, Li X, Zhang N, et al · · 2023 · cited 246× · PMID 37669923 · DOI 10.1038/s41392-023-01589-z
  3. Expanding PROTACtable genome universe of E3 ligases.
    Liu Y, Yang J, Wang T, Luo M, et al · · 2023 · cited 117× · PMID 37845222 · DOI 10.1038/s41467-023-42233-2
  4. Targeted protein degradation: advances in drug discovery and clinical practice.
    Zhong G, Chang X, Xie W, Zhou X. · · 2024 · cited 112× · PMID 39500878 · DOI 10.1038/s41392-024-02004-x
  5. The BCL2 family: from apoptosis mechanisms to new advances in targeted therapy.
    Vogler M, Braun Y, Smith VM, Westhoff MA, et al · · 2025 · cited 104× · PMID 40113751 · DOI 10.1038/s41392-025-02176-0
  6. Clinical considerations for the design of PROTACs in cancer.
    Nieto-Jiménez C, Morafraile EC, Alonso-Moreno C, Ocaña A. · · 2022 · cited 71× · PMID 35249548 · DOI 10.1186/s12943-022-01535-7
  7. Overcoming Gemcitabine Resistance in Pancreatic Cancer Using the BCL-X<sub>L</sub>-Specific Degrader DT2216.
    Thummuri D, Khan S, Underwood PW, Zhang P, et al · · 2022 · cited 61× · PMID 34667112 · DOI 10.1158/1535-7163.mct-21-0474
  8. Targeting the histone H3 lysine 79 methyltransferase DOT1L in MLL-rearranged leukemias.
    Yi Y, Ge S. · · 2022 · cited 53× · PMID 35331314 · DOI 10.1186/s13045-022-01251-1

Verify or expand the search:

Other trials of DT2216

Trials testing the same drug.

Other recruiting trials for Solid Tumor

Currently open trials in the same condition.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04886622.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing