Expertise in
1
conditions

Dr. Cori L. Daines

Pediatric Pulmonology | Pediatrics | Pulmonary Medicine
Banner-University Medical Group
707 N Alvernon Way, Suite 301, 
Tucson, AZ 
Accepting New Patients
Offers Telehealth
Expertise in
1
conditions
Banner-University Medical Group
707 N Alvernon Way, Suite 301, 
Tucson, AZ 
OverviewInsuranceLocationsClinical ResearchSimilar Doctors

Overview

Cori Daines is a Pediatric Pulmonologist and a Pediatrics provider in Tucson, Arizona. Mrs. Daines is highly rated in 1 condition, according to our data. Her top areas of expertise are Cystic Fibrosis, Pseudomonas Stutzeri Infections, Duchenne Muscular Dystrophy, and High Blood Pressure in Infants. Mrs. Daines is currently accepting new patients.

Her clinical research consists of co-authoring 41 peer reviewed articles and participating in 6 clinical trials. MediFind looks at clinical research from the past 15 years.

Specialties
Pediatric Pulmonology
Pediatrics
Pulmonary Medicine
Licenses
Pediatric Pulmonology in OH
Languages Spoken
English
Gender
Female

Insurance

Accepted insurance can change. Please verify directly with the provider.

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Accepted insurance plans:

Cigna
  • EPO
  • HMO
  • PPO
Humana
  • HMO
  • INDEMNITY
  • POS
  • PPO
UnitedHealthcare
  • EPO
  • HMO
  • POS
  • PPO

Locations

BANNER-UNIVERSITY MEDICAL GROUP
707 N Alvernon Way, Suite 301, Tucson, AZ 85711
Other Locations
BANNER-UNIVERSITY MEDICAL GROUP
535 N Wilmot Rd, Suite 101, Tucson, AZ 85711

Clinical Research

Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Providers who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.

6 Clinical Trials

Streamlined Treatment of Pulmonary Exacerbations in Pediatrics (Pilot)
Streamlined Treatment of Pulmonary Exacerbations in Pediatrics (Pilot)
Enrollment Status: Completed
Publish Date: October 18, 2024
Intervention Type: Other
Study Drug: Antibiotics
Study Phase: Not Applicable
A Phase III Double-blind, Randomized, Placebo-Controlled Study Assessing the Efficacy, Safety and Tolerability of Idebenone in Patients With Duchenne Muscular Dystrophy Receiving Glucocorticoid Steroids
A Phase III Double-blind, Randomized, Placebo-Controlled Study Assessing the Efficacy, Safety and Tolerability of Idebenone in Patients With Duchenne Muscular Dystrophy Receiving Glucocorticoid Steroids
Enrollment Status: Terminated
Publish Date: December 03, 2021
Intervention Type: Drug
Study Drug: Idebenone
Study Phase: Phase 3
A Phase III Open-Label Extension Study to Assess the Long-Term Safety and Efficacy of Idebenone in Patients With Duchenne Muscular Dystrophy (DMD) Who Completed the SIDEROS Study
A Phase III Open-Label Extension Study to Assess the Long-Term Safety and Efficacy of Idebenone in Patients With Duchenne Muscular Dystrophy (DMD) Who Completed the SIDEROS Study
Enrollment Status: Terminated
Publish Date: December 03, 2021
Intervention Type: Drug
Study Drug: Idebenone
Study Phase: Phase 3
Feasibility of a Mobile Medication Plan Application in CF Patient Care
Feasibility of a Mobile Medication Plan Application in CF Patient Care
Enrollment Status: Completed
Publish Date: August 03, 2021
Intervention Type: Behavioral
Study Phase: Not Applicable
A Randomized, Double-Blind, Parallel Group, Placebo-Controlled Study Investigating the Optimal Dose Regimen, Efficacy, and Safety of Adding Oral Cysteamine in Adult Patients Being Treated for an Exacerbation of CF-associated Lung Disease
A Randomized, Double-Blind, Parallel Group, Placebo-Controlled Study Investigating the Optimal Dose Regimen, Efficacy, and Safety of Adding Oral Cysteamine in Adult Patients Being Treated for an Exacerbation of CF-associated Lung Disease
Enrollment Status: Completed
Publish Date: April 14, 2021
Intervention Type: Drug
Study Phase: Phase 2
A Phase 2, Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel-group Study to Evaluate the Efficacy, Safety, and Tolerability of CTX-4430 Administered Orally Once-Daily for 48 Weeks in Adult Patients With Cystic Fibrosis
A Phase 2, Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel-group Study to Evaluate the Efficacy, Safety, and Tolerability of CTX-4430 Administered Orally Once-Daily for 48 Weeks in Adult Patients With Cystic Fibrosis
Enrollment Status: Completed
Publish Date: September 04, 2019
Intervention Type: Drug
Study Phase: Phase 2
View 5 Less Clinical Trials

41 Total Publications

Long-Term Safety and Efficacy of Elexacaftor/Tezacaftor/Ivacaftor in Adults and Adolescents with Cystic Fibrosis and at Least One F508del Allele: A Phase 3, Open-Label Extension Study.
Long-Term Safety and Efficacy of Elexacaftor/Tezacaftor/Ivacaftor in Adults and Adolescents with Cystic Fibrosis and at Least One F508del Allele: A Phase 3, Open-Label Extension Study.
Journal: American journal of respiratory and critical care medicine
Published: April 10, 2025
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1625 N Campbell Ave, 
Tucson, AZ 
 (2.3 mi)
520-694-0111
Languages Spoken:
English, Hindi
See accepted insurances
Accepting New Patients
Offers Telehealth

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Areas of Expertise

MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.

Learn more about MediFind’s expert tiers

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