Indication intelligence, analysis and sector perception

RMi Research Note: Capricor Therapeutics (CAPR) I am NOT the ONLY dissenter

December 18, 2025

Thursday, CAPR yells as the roller-coaster crests-up, now waiting for the downslide groan! Opened -$0.04, flipped +$0.66, mid-day to -$0.02 closing at +$0.04. Doubts still abound re: regulatory fragility and marginal HOPE-3 results and valuation concerns remain a key hang-up! CAPR remains a structurally challenged, chronically unprofitable company whose valuation is disconnected from fundamentals. Despite years of promoting Deramiocel (CAP-1002) as a potential treatment for Duchenne muscular dystrophy (DMD); CAPR has yet to generate any meaningful/partnering revenue only losses, relying on repeated capital raises and marketing narratives to sustain operations.

RMi Research Note: Harvard Apparatus GT (OTCQB:HRGN): I reiterate WHO is pumping the volume and share pricing?

December 12, 2025

Who is wasting lipstick on this pig? WHO and WHAT is CONNING “American” investors re Harvard Apparatus RT (OTVQB: HRGN), a Beijing, China percentage “owned” and run company … Patterns of share pricing manipulation? OTCQB: HRGN traded 12/11... +$0.12 with 4,615 shares traded after Thursday’s $0.00, Wednesday’s -$0.06 with 600 shares traded, Tuesday’s $0.00 with 600 shares traded and Monday’s (12/8) +$0.18 with 6,900 shares traded) – manipulating the downside, PONZI scheme? Cash starved, NO clinical data after 5-year ago IND. Accumulated deficit to date= $103.2 M in 12 years U.S. investors BEWARE, forewarned is forearmed?              

RegMedInvestors (RMi) Financing: Capricor Therapeutics (CAPR) prices offering of 6 M shares at $25.00 per share with ... skepticism!

December 5, 2025

CAPR is trading +1.00 at $26.32 The offering to close on or about 12/8/25. CAPR believes these pivotal study results, in addition to the evidence from the HOPE-2 and HOPE-2 OLE studies, position … clinical issues in the FDA’s Complete Response Letter received earlier this year, consistent with prior FDA guidance that HOPE-3 results should be sufficient to support regulatory approval.” However, there are significant execution and regulatory risks around Deramiocel, including shifting FDA guidance and development costs.