Meet PharPoint: The CRO of Choice for Emerging, Innovative Companies

With attentive support, an experienced team, faster biometrics timelines, and full-service CRO capabilities, PharPoint Research can help Aldena Therapeutics meet study goals.

PharPoint has successfully supported 180+ Sponsors and has never had a study pulled due to poor quality.

“There is an inherent honesty and authenticity in [PharPoint’s] approach. …I have complete faith and trust in PharPoint as our partner, and that gives me confidence in the success of our clinical program.”

CLIENT TESTIMONIAL

“High priority pivotal studies locked and delivered faster than any other CRO I have worked with in my experience. Not only was the study delivered within budget and early, it was a quality deliverable.”

CLIENT TESTIMONIAL

PharPoint is a full-service contract research organization that helps innovative sponsors meet their clinical trial goals.

AN EXPERIENCED TEAM

With PharPoint as your CRO, your study is always in good hands. We align our clients with attentive study teammates who have proven expertise that aligns with Aldena Therapeutic’s upcoming trials.

A BETTER PARTNER

Work with a CRO you can trust. At PharPoint, we’re all about creating a better relationship between CRO and Sponsor: one that’s transparent, communicative, consultative, and aligned for study success.

YOUR GOALS: MET

Faster timelines, quality deliverables, and a proactive approach to risk mitigation allow us to help you meet your clinical trial goals quickly and cost effectively.

SUCCESS STORY

A dermatology study enrolled five months early

PharPoint provided clinical and biometrics support for a US-based Phase 2 dermatology study, ultimately helping our client meet enrollment goals five months early despite closures due to COVID-19.

PharPoint worked collaboratively with Sponsor, sites, and other key study partners to allow the study to progress efficiently and enroll rapidly. A specialized patient recruitment partner was brought on, providing additional enrollment support to study sites. PharPoint’s attentive, supportive site relationships kept us – and the study Sponsor – in front-row seats to study progress, closely monitoring and responding to missed visits.

Discover what makes PharPoint the right CRO for Aldena Therapeutic’s clinical trial outsourcing needs.

PharPoint has supported over 1,000 clinical trials, including trials within dermatology and immuno-inflammatory indications.

 

Some of our experience highlights include:

  • 120+ dermatology and immunology trials supported across 25+ indications
  • Clinical PMs with 10+ years experience
  • Biostatisticians all have advanced degrees
  • 175+ databases built by our data management team

Unlike big-box CROs that can sometimes leave smaller Sponsors feeling overlooked and forgotten, PharPoint looks at Sponsor-CRO relationships as a partnership, prioritizing your study data and goals.

This includes access to a study-aligned, attentive, and experienced team along with clear escalation pathways. From the very start, PharPoint prioritizes your study and study data (allowing us to provide rapid study results following last patient, last visit).

Aldena Therapeutics can get study results faster according to PharPoint’s industry-best biometrics timelines.

 

Highlights from our standard timeline include:

  • Database lock 5 days after LPLV SDV (compared to industry standard of 36 days)
  • Top line results 2 days after database lock
  • Draft TLFs 3 days after the delivery of top line results
  • CSR delivered within 40 business days of top line results

Our team has experience across a range of indications, including:

Acne

Alopecia

Atopic Dermatitis

Cutaneous Lupus Erythematosus

Epidermolysis Bullosa

Hair Loss

Lipoma

Lupus

Onychomycosis

Psoriasis

Scleroderma

Sjogren-Larsoon Syndrome

Submental Subcutaneous Fat

Vitiligo

Venous Leg Ulcers

Learn how we can help you meet study goals.
Schedule 15 minutes with PharPoint


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