Indero supports late stage clinical development, empowering dermatology and rheumatology researchers to demonstrate efficacy and safety through phase 2b-3 studies.
Manage Costs & Mitigate Risks With Late Phase Clinical Research
Inderoâs dermatology and rheumatology experts evaluate protocol and recruitment objectives to ensure the successful execution of late phase trials. With extensive site connections across the globe and the ability to handle large, multicenter studies, Indero can get your study where it needs to goâmeeting your timelines and quality requirements.
Late Phase Studies
225+
Clinical Trials
475+
Investigators
2975+
Indications
25+
Late Phase Study Capabilities
Late phase studies provide critical insights into long-term safety, efficacy, and real-world applications, ensuring treatments meet regulatory and patient needs. Inderoâs extensive experience in dermatology and rheumatology trials and deep understanding of immune-mediated conditions positions us as a trusted partner for late phase studies at scale.
Project Management
Our project managers have extensive dermatology and rheumatology experience in all phases of clinical trials, offering leadership and support to sponsors at every stage.
Site Network
We have strong relationships with sites across the world that can meet your requirements for everything from recruitment and retention to timelines and quality.
Innovative Patient Recruitment
We have a dedicated patient recruitment and advertising team working alongside our project management team to build innovative strategies specifically customized for your late phase clinical trials.
Clinical Monitoring
Indero has a team of Clinical Research Associates (CRAs) with capabilities to support all sites in North America, Europe, Latin America, and Asia Pacific. This allows us to rapidly assemble a flexible monitoring team depending on site location, project needs, and monitoring plan requirements.
Geographical Footprint
Inderoâs integrated services span the entire world, with capabilities in North America, Europe, Latin America, and Asia Pacific. Wherever you need to take your trial to ensure genetic diversity among subjects, we can support you.
Biometrics
Indero uses validated and robust in-house data management systems to deliver customized biometrics services. We focus on understanding the sponsorâs goals and study objectives, which ensures the ideal methods for data collection and analysis.
Late Phase Study Services
Late phase clinical trials help dermatology and rheumatology researchers assess the market readiness of new treatments and monitor for potential long-term side effects at scale. Indero specializes in delivering comprehensive solutions for late phase trials, providing robust evidence of a drugâs efficacy and safety in a diverse patient population. Our services include:
âThe expertise and motivation Indero brought to the table were pivotal to our success. From the initial synopsis development to the final stages of study conduct, the synergy between our teams was palpable and was underpinned by Innovadermâs strong relationships with sites, investigators, and KOLs.â
 Dermatology & Rheumatology Indications for Late Phase Studies
Indero can support late phase studies across a wide range of dermatology and rheumatology indications, including:
Atopic dermatitis
Psoriasis
Alopecia areata
Hidradenitis suppurativa
Chronic inducible urticaria
Chronic spontaneous urticaria
Vitiligo
Acne
Rosacea
Chronic hand eczema
Notalgia paresthetica
Actinic keratosis
GPP, PPP, and PPPP
Hyperhidrosis
Prurigo nodularis
Onychomycosis
Cosmetics and aesthetics
Rheumatoid arthritis
Osteoarthritis
Radiographic (ankylosing spondylitis) and non-radiographic axial spondyloarthritis
Psoriatic arthritis
Systemic lupus erythematosus (SLE) and juvenile SLE
Lupus nephritis
Idiopathic inflammatory myopathies, including polymyositis and dermatomyositis
Sjögren’s disease
Systemic sclerosis (scleroderma)
Osteoporosis
Atopic Dermatitis Phase 3 Study Reaches 200% Enrollment within First 5 Months
Indero successfully managed a Phase 3 atopic dermatitis program testing a topical treatment, which included four studies across the USA, Canada, and Europe.
Challenges
Site selection:Â
Very competitive and saturated indication in North America
Recruitment:Â
Recruitment slowed down after open-label extension (OLE) enrollment was completed
Photography:
Material shipment and site training impacted siteâs activation timelines
Strategy
Evaluated expansion in other regions than North America
Supplement site recruitment activities with substantial digital central advertisement programs
Conducted follow-up with sites to ensure photograph training was completed on schedule
Shipped photography material in conjunction with site contract signature for a streamlined activation timeline
Wherever Youâre Going, Weâre all in.
Need help with your next study? We want to learn more. Fill out the form on the right and one of our experts will be in touch.
Inderoâs Early Phase 1 model enables sponsors to initiate topical studies that detect early pharmacodynamic signals much sooner than traditional phase 1, using microdosing and transcriptomic analysis. This approach reduces preclinical requirements, shortens study duration from 8â12 weeks to â€3 days, and lowers costs, helping teams make informed go/no-go decisions faster.
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