Telik

21 total trials 16 completed

Telik sponsors 21 registered US clinical trials on ClinicalTrials.gov, none currently recruiting, and 16 completed. 4 of these trials are in Phase 3-4 (later-stage) and 17 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Non-Small-Cell Lung Carcinoma, with 1 trials.

Trial Pipeline

21 total, page 1 of 1

TERMINATED Phase 2

Phase 2 Study of Telintra® in Deletion 5q Myelodysplastic Syndrome

NCT01422486

TERMINATED Phase 2

Study of (Telintra®) in Non-Del(5q) Myelodysplastic Syndrome

NCT01459159

COMPLETED Phase 2

Study of Canfosfamide in Refractory or Relapsed Mantle Cell, Diffuse Large B Cell Lymphoma and Multiple Myeloma

NCT01148108

COMPLETED Phase 1

Dose-Ranging Study of Telintra® Tablets + Revlimid® in Patients With Non-Deletion (5q) Low to Intermediate-1 Risk Myelodysplastic Syndrome (MDS)

NCT01062152

TERMINATED Phase 2

Study of Ezatiostat (Telintra Tablets) for Treatment of Severe Chronic Neutropenia

NCT00909584

TERMINATED Phase 2

Study of Telintra for Treatment of Chemotherapy Induced Neutropenia in Patients With Non-Small Cell Lung Cancer

NCT00701870

COMPLETED Phase 2

Phase 2 Study Comparing Two Dose Schedules of Telintra™ in Myelodysplastic Syndrome (MDS)

NCT00700206

TERMINATED Phase 3

Phase 3 Randomized Study of Telcyta + Doxorubicin Versus Doxorubicin in Platinum Refractory or Resistant Ovarian Cancer

NCT00350948

COMPLETED Phase 1

Study of TLK199 Tablets in Myelodysplastic Syndrome (MDS)

NCT00280631

COMPLETED Phase 3

TLK286 (Telcyta) in Combination With Carboplatin (Paraplatin) Versus Doxil in Platinum Refractory or Resistant Ovarian Cancer

NCT00102973

COMPLETED Phase 1

Carboplatin, Paclitaxel and TLK286 (Telcyta) as First-Line Therapy in Advanced Non-Small Cell Lung Cancer

NCT00088556

COMPLETED Phase 1

TLK286 (Telcyta) in Combination With Cisplatin for Locally Advanced or Metastatic Non-small Cell Lung Cancer (NSCLC)

NCT00077883

COMPLETED Phase 3

TLK286 (Telcyta) vs. Doxil/Caelyx or Hycamtin in Platinum Refractory or Resistant Ovarian Cancer

NCT00057720

COMPLETED Phase 1

TLK286 in Combination With Doxil in Platinum Refractory or Resistant Ovarian Cancer

NCT00052065

COMPLETED Phase 1

TLK286 in Combination With Paraplatin (Carboplatin) in Recurrent Ovarian Cancer

NCT00051948

COMPLETED Phase 1

Phase 1-2a Dose-Ranging Study of TLK286 in Combination With Docetaxel in Platinum-Resistant Non-Small Cell Lung Cancer

NCT00047801

COMPLETED Phase 2

Phase 2 Study of TLK286 Administered Weekly in Advanced Non-Small Cell Lung Cancer

NCT00040638

COMPLETED Phase 2

Phase 2 Study of TLK286 in Metastatic Breast Cancer

NCT00035841

COMPLETED Phase 1

Study of TLK199 HCl Liposomes for Injection in Myelodysplastic Syndrome

NCT00035867

COMPLETED Phase 2

Phase 2 Study of TLK286 in Platinum Resistant Advanced Epithelial Ovarian Cancer

NCT00038428

COMPLETED Phase 3

Study of TLK286 (Telcyta) vs. Gefitinib in Locally Advanced or Metastatic Non-Small Cell Lung Cancer

NCT00080340

Phase Distribution

PhaseTrial count
Phase 1 8
Phase 2 9
Phase 3 4

What the Pipeline for Telik Shows

According to the ClinicalTrials.gov registry, Telik is linked to 21 US clinical trials across every stage of research activity. Of those, 0 studies are currently recruiting, about 0% of the sponsor's indexed portfolio, and 16 are already marked complete, representing roughly 76% of the total.

The phase mix for Telik reports 4 late-stage studies (Phase 3 and Phase 4 combined) and 17 earlier-phase studies (Phase 1 and Phase 2).

The top therapeutic focus area indexed for Telik is Non-Small-Cell Lung Carcinoma with 1 linked trial, and 1 other condition area appear in the top list above.

How to read these pipeline numbers

Recruiting share is one of the more practical signals here: it reflects how much of a sponsor's research is presently open to new participants, while the completed share indicates the depth of finished work that has already contributed registry results. Both counts come directly from the public ClinicalTrials.gov dataset and are refreshed on the registry side; this page mirrors the latest data pull without altering it.

A portfolio weighted toward Phase 3 usually reflects an organization advancing candidates toward regulatory review, where the research centers on comparative efficacy and broader safety across larger populations. A heavier Phase 1 and Phase 2 tilt generally indicates exploratory work, safety, dosing, and early signal detection, and is common among research-forward sponsors that seed many early programs. Phase 4 entries, when present, track interventions already in real-world use and typically focus on long-term safety, effectiveness across subgroups, or formulation comparisons.

That distribution is a quick read of where the organization concentrates its research attention; it does not imply product availability, market share, or any clinical endorsement. All numbers on this page come from ClinicalTrials.gov maintained by the National Library of Medicine, and counts can shift as new studies are registered or existing ones update their status. This information is provided for reference and educational purposes only, not as medical, investment, or regulatory advice, verify current details directly with ClinicalTrials.gov before relying on any figure here.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page aggregates every registered trial from this sponsor, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.