CClinicalTrials.gg
AvailableNCT07000695Updated Jun 18, 2026

Managed Access Programs for TQJ230, Pelacarsen

An expanded access record providing Pelacarsen in Atherosclerotic Cardiovascular Disease, ASCVD, sponsored by Novartis Pharmaceuticals. Available. Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2026-06-18.

Sponsored by Novartis Pharmaceuticals (part of Novartis) · Expanded access

Study type
Expanded access
Access type
Intermediate-size population
Ages
18 Years to 80 Years
Sex
All
01

Study summary

The purpose of this registration is to list Managed Access Programs (MAPs) related to TQJ230, pelacarsen

Read the detailed description

CTQJ230A12013M - Available - Managed Access Program (MAP) Cohort Treatment Plan (CTQJ230A12013M) to provide access to pelacarsen (TQJ230) for (Atherosclerotic Cardiovascular Disease, ASCVD)

02

Conditions studied

  • Atherosclerotic Cardiovascular Disease, ASCVD

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Keywords

  • MAP
  • Manage Access Program
  • TQJ230
  • Pelacarsen
  • Atherosclerotic Cardiovascular Disease
  • ASCVD
03

In context

Atherosclerosis

1,568 studies on the registry are indexed under Atherosclerosis; 264 are open to participants now.

Browse Atherosclerosis studies →

Lead sponsor

Novartis Pharmaceuticals is the lead sponsor of 2,673 studies on the registry; 228 are open to participants now.

Of its 576 completed or terminated interventional studies of FDA-regulated products, 431 (75%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

Inclusion Criteria:

  1. An independent request was received from a licensed physician.
  2. The patient has a serious or life-threatening disease or condition and there is no comparable or satisfactory alternative therapy available for diagnosis, monitoring, or treatment.
  3. The patient is not eligible or able to enrol in a clinical trial or continue participation in such trial.
  4. There is a potential patient benefit to justify the potential risk of the treatment use, and the potential risk is not unreasonable in the context of the disease or condition to be treated.
  5. The patient must meet any other medical criteria established by the medical experts responsible for the product or by the health authority in the country of request (as applicable).
  6. Provision of the product will not interfere with the initiation, conduct, or completion of a Novartis clinical trial or overall development program.
  7. Managed Access provision is allowed per local laws/regulations.
05

Access details

Study type
Expanded access
Access type
Intermediate-size population

Available treatment

  • DrugPelacarsen

    Patients receive Pelacarsen

    Also known as: TQJ230

06

Where to request access

No study locations are listed for this record.

07

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 18, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
08

Registry details

Key details

Study ID
NCT07000695
Responsible party
Sponsor
First posted
Jun 3, 2025
Last update
Jun 18, 2026

Study contacts

Novartis Pharmaceuticals
Contact
novartis.email@novartis.com
+41613241111
Novartis Pharmaceuticals
Contact
View the source record on ClinicalTrials.gov ↗

Requesting access

Expanded access is arranged between your doctor and the company. Ask your care team to contact the provider listed on this record.

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