[No standalone website (unbranded, no questionnaire)] A Study of Subjects With Psoriatic Arthritis to Investigate the Effectiveness of Adalimumab Introduction Compared With Methotrexate Dose Escalation (CONTROL)

How to apply

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Study’s contact

Call center

+81-3-6225-1111(M-F 9-5 JST)

Email address

dsclinicaltrial@daiichisankyo.co.jp

Condition

Advanced Cancer,Metastatic Solid Tumor,Solid Tumor

Treatment type

Interventional

Investigational product

DS-1055a

Phase

Phase 1

Sponsor

Daiichi Sankyo, Inc.

ClinicalTrials.gov identifier

NCT04419532

Study number

DS1055-A-J101

Understanding clinical trials

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About the study

The purpose of this study is to assess the safety and tolerability of DS-1055a in participants with relapsed or refractory locally advanced or metastatic solid tumors for which no standard treatment is available.

Who can take part?

You may be eligible to participate in the study if you meet the following criteria:

Inclusion criteria

  1. Has a histopathologically documented locally advanced or metastatic head and neck, gastric, esophageal cancer, non-small cell lung cancer, or melanoma. Participants with other types of solid tumors may be eligible following discussion with the Sponsor.
  2. Has a relapsed or refractory disease that is not amenable to curative standard therapy.
  3. Is 18 years of age or older.
  4. Has an Eastern Cooperative Oncology Group Performance Status (ECOG PS) of 0-1, with no deterioration for two weeks.
  5. Has a measurable disease based on Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1.
  6. Has adequate organ function within 7 days before enrollment.
  7. Is able to provide written informed consent and is willing and able to comply with the protocol.
Exclusion criteria

  1. Has a concurrently active second malignancy, other than adequately treated non-melanoma skin cancers, in situ melanoma or in situ cervical cancer. Participants with history of the second malignancy have been disease-free for <3 years.
  2. Has a history of (non-infectious) interstitial lung disease (ILD) that required steroids, currently has ILD, or when suspected ILD cannot be ruled out by imaging at screening.
  3. Has a history of severe pulmonary compromise or requirement of supplemental oxygen within 6 months before enrollment.
  4. Has active hepatitis B or hepatitis C virus infection.
  5. Has received prior immunotherapy with a Grade 3 or higher, or any unresolved ≥Grade 2 immune-related adverse event.

For a full list of inclusion/exclusion criteria, please visit ClinicalTrials.gov

Study locations

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How to apply

Determine if a study site for this clinical trial is near you. Contact the study to apply.

Find a Study Site