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Creative Medical Technology Holdings Reaches Major Clinical Inflection Point with Positive Interim Data from ADAPT Trial and CELZ-201 (Olastrocel) in the Treatment of Chronic Lower Back Pain

Key Takeaway: Creative Medical Technology Holdings announced positive interim results from its ADAPT trial for CELZ-201 (Olastrocel), a cell therapy for chronic lower back pain. The trial showed significant improvements in functional disability and pain, confirming its efficacy and safety. The company is now focusing on regulatory engagement and commercialization planning.
Price reaction · baseline $2.05 (2026-01-12 close) · hit pre-market · clean, no other CELZ news in the window
day 0 close
-11.2%
day 1
-9.8%
day 3
-2.4%

Market Sentiment Analysis

POSITIVE FACTORS

  • Positive interim data from ADAPT trial shows significant improvements.
  • CELZ-201 (Olastrocel) has an excellent safety profile with no significant adverse events.
  • The treatment addresses a large market with high unmet medical needs.

BiopharmaWatch Analysis

From our catalyst data and publicly available data · not financial advice
Best trade, last catalyst
+79%
120-day peak, hindsight
Typical move
34.3%
average across 2 past catalysts
Cash runway
~17 mo
Low dilution risk
Lead asset
CELZ-201 Administration
Phase 1 · Type 1 Diabetes

Full Press Release Details

PHOENIX, Jan. 13, 2026 (GLOBE NEWSWIRE) --Creative Medical Technology Holdings, Inc. (NASDAQ: CELZ) (“Creative Medical” or the “Company”), a clinical-stage biotechnology company advancing regenerative medicine solutions, today announced positive interim 180-day follow-up data from its FDA-cleared ADAPT clinical trial evaluating CELZ-201 (Olastrocel), the Company’s proprietary perinatal tissue-derived cell therapy for chronic lower back pain associated with degenerative disc disease.
The study produced statistically significant, clinically meaningful improvements in both functional disability (ODI%) and pain at primary trial end point, confirming durable human efficacy alongside an excellent safety profile.
The announcement of this data follows a previously announced study enrollment completion and positive independentData Safety Monitoring Board (DSMB) safety review, which confirmed that CELZ-201(Olastrocel) demonstrated a favorable safety profile with no significant adverse events and supported continued advancement of the trial.
“We view this as a major corporate and clinical inflection point for Creative Medical, reflecting the transition of CELZ-201 (Olastrocel) from a clinical program into a promising strategic asset,” said Timothy Warbington, President and CEO. “Our focus is execution, data transparency, and unlocking the full value of this platform for patients and shareholders.”

Key Clinical Outcomes at Interim Analysis

Market Opportunity & DifferentiationChronic lower back pain affects more than 16 million Americans and represents a multi-billion-dollar annual market. Current standards of care rely heavily on opioids, steroid injections, or invasive spine surgery, with limited durable solutions. CELZ-201 (Olastrocel) is an off-the-shelf, allogeneic regenerative cell therapy designed to deliver scalable, consistent, non-surgical, disease-modifying benefit.
Strategic Positioning & Next CatalystsWith safety de-risked and human efficacy signals, CELZ-201 (Olastrocel) is transitioning from execution risk to a data-driven value creation phase. The Company is advancing toward late-stage regulatory engagement, strategic partnership discussions, and commercialization planning awaiting final data.
About Creative Medical Technology Holdings, Inc.Creative Medical Technology Holdings, Inc. (NASDAQ: CELZ) is a clinical-stage biotechnology company pioneering regenerative medicine therapies derived from adult and perinatal stem cell technologies. The Company’s pipeline targets large, underserved markets across orthopedics, immunotherapy, endocrinology, urology, and gynecology, with a mission to deliver scalable, disease-modifying solutions for patients with high unmet medical needs.
For more information, visitwww.creativemedicaltechnology.com
Forward-Looking StatementsThis press release contains forward-looking statements regarding clinical development, regulatory strategy and positioning, commercialization potential, and market opportunity. These statements are based on current expectations and involve risks and uncertainties that could cause actual results to differ materially. Factors include clinical trial outcomes, regulatory decisions, manufacturing considerations, competitive dynamics, and market conditions. Please refer to the Company’s filings with the SEC for a discussion of these risks. The Company undertakes no obligation to update forward-looking statements except as required by law.

Investor & Media Contacts

Investor RelationsDevin Sullivan — The Equity Group Inc.dsullivan@theequitygroup.com

Conor Rodriguez — The Equity Group Inc.crodriguez@theequitygroup.com

RedChip CompaniesDave Gentry —CELZ@redchip.com| 1-407-644-4256Paul Kuntz —paul@redchip.com| 412-708-4590

Frequently Asked Questions

What is CELZ-201 (Olastrocel)?

CELZ-201 (Olastrocel) is a perinatal tissue-derived cell therapy for chronic lower back pain.

What were the results of the ADAPT trial?

The ADAPT trial showed significant improvements in functional disability and pain at the primary endpoint.

What is the safety profile of CELZ-201?

CELZ-201 demonstrated an excellent safety profile with no significant adverse events reported.

What is the market opportunity for CELZ-201?

Chronic lower back pain affects over 16 million Americans, representing a multi-billion-dollar market.

What are the next steps for Creative Medical Technology?

The company is focusing on regulatory engagement, strategic partnerships, and commercialization planning.

Last updated: Jan 13, 2026