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A Long-Term Safety and Efficacy Study of Verekitug (UPB-101) in Adult Participants With Severe Asthma (VALOUR)

RECRUITINGPhase 2Sponsored by Upstream Bio Inc.
Actively Recruiting
PhasePhase 2
SponsorUpstream Bio Inc.
Started2025-05-21
Est. completion2027-09
Eligibility
Age18 Years+
Healthy vol.Accepted
Locations26 sites

Summary

The primary purpose of this study is to evaluate the long-term safety and efficacy of verekitug (UPB-101) in participants who complete the VALIANT study (NCT06196879).

Eligibility

Age: 18 Years+Healthy volunteers accepted
Inclusion Criteria:

1. Completion of the VALIANT study (UPB-CP-04 \[NCT06196879\]) per protocol.
2. Participant has signed, dated, and received a copy of the Institutional Review Board (IRB)/Independent Ethics Committee (IEC)-approved written informed consent form (ICF) for the LTE study.
3. Contraceptive use by participants must be consistent with local regulations regarding the methods of contraception for those participating in clinical studies.

Exclusion Criteria:

1. Abnormal medical history, physical finding, or safety finding that in the opinion of the Investigator may obscure the study data or interfere with the participant's safety.
2. Any clinical laboratory test result outside of the reference ranges considered by the Investigator as clinically significant and that may obscure the study data or interfere with the participant's safety.
3. Participant with a history or evidence of a clinically significant pulmonary condition (other than asthma), including significant restrictive findings on pulmonary function testing, chronic bronchitis, emphysema, bronchiectasis, pulmonary fibrosis, or any other related condition that may obscure the study data (e.g., gastroesophageal reflux and vocal cord paralysis/dysfunction).
4. Pregnant or breastfeeding or planning to become pregnant or breastfeed during the study or unwilling to use adequate birth control, if of reproductive potential and sexually active.
5. Participants with significant protocol deviations in VALIANT, assessed at the discretion of the Sponsor.
6. Participant is unreliable, incapable of adhering to the protocol and visit schedule according to the judgment of the Investigator or has any disorder that may compromise their ability to give informed consent.

Conditions2

AsthmaSevere Asthma

Locations26 sites

Kern Research, Inc.
Bakersfield, California, 93301
California Medical Research Associates Inc.
Northridge, California, 91324
Integrated Research of Inland Inc
Upland, California, 91786
Allergy & Asthma Clinical Research
Walnut Creek, California, 94598
Allianz Research Institute
Westminster, California, 92683

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