Neoadjuvant Pembrolizumab and Porustobart in Resectable pMMR/MSS Colon Cancer

Trial statusNot yet recruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorSolstice Oncology, Inc.

About this trial

The goal of this clinical trial is to learn if giving two medicines together, porustobart and pembrolizumab, before surgery can treat a common type of colon cancer called microsatellite stable (MSS) colon cancer in adults. This type of cancer can be removed with surgery and has not spread to other parts of the body. Both medicines work by helping the immune system fight cancer.

The main questions this study wants to answer:

How well do the medicines destroy the cancer before surgery? What side effects do participants have when taking the medicines?

Researchers will compare two groups to see which treatment schedule works better and is safer. Both groups get pembrolizumab. One group gets one dose of porustobart (Day 1 only), and the other group gets two doses (Day 1 and Day 22).

Participants will:

Complete certain tests and procedures to make sure they are eligible Get the medicines through a vein on Day 1 and Day 22 then have surgery 6-9 weeks after starting treatment Return for checkups and tests every 6 months for up to 3 years after surgery

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

None

Disqualifiers

None

Trial design

Design model

Parallel

Treatments tested in this trial

  • Pembrolizumab

    Drug

    Administered to: Arm 1, Arm 2

  • Porustobart

    Drug

    Administered to: Arm 1, Arm 2

Treatment groups

100 Participants
are divided into 2 treatment groups
Group A: Arm 1Experimental treatment 2 interventions
Group B: Arm 2Experimental treatment 2 interventions

Trial outcomes

Primary outcomes

1

Major Pathologic Response (MPR) rate by Blinded Independent Pathologic Review (BIPR)

MPR is defined as the proportion of patients with ≤10% residual tumor volume in the primary tumor and lymph nodes, as evaluated by BIPR, per treatment arm

Time frame
Assessed from surgical resection specimen (surgery occurs Day 42-Day 63, i.e., approximately Week 6-Week 9 after first dose)

Secondary outcomes

1

Pathologic Complete Response (pCR) rate

Time frame
Assessed from surgical resection specimen (Week 6-9)
2

Incidence of treatment-related adverse events (AEs), serious adverse events (SAEs), and immune-related AEs

Time frame
From informed consent through 60 days after last dose (or initiation of new anti-cancer treatment, whichever occurs first)

Other outcomes

Sponsors and contacts

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This trial is not recruiting at the moment. You can still explore other options: