AbbVie Wins EU Nods; Moderna Surges 125% YTD

CHMP backs RINVOQ expansion while diagnostics makers advance glucose biosensing; China leads oncology trials with 40% global share

Money365.Market AI
3 min read
Market MoodCautious
Sentiment+35Mixed

Key DriverRegulatory momentum from European CHMP opinions and FDA clearances offset by persistent inflation headwinds affecting broader equities

Today in 30 Seconds

  • AbbVie secures positive CHMP opinions for RINVOQ in alopecia areata & vitiligo
  • Moderna up 125.51% YTD on FDA flu vaccine approval & pipeline expansion
  • DexCom gains FDA clearance for Stelo in children ages 2+; China leads 40% oncology trials

Top Movers

$MRNA +125.5%

Moderna

FDA flu vaccine win, corporate pivot, expanding pipeline

$UNH +10.0%

UnitedHealth Group

Gained over past 30 days, trading near 52-week high

$LLY +6.0%

Eli Lilly

30-day gain with Street expecting 13.6% upside

All Briefs

Big Pharma & Biotech

Bullish

Moderna YTD gain

125.51%+125.51%

Eli Lilly 30-day gain

6%+6%

China oncology trial share

40%

RINVOQ alopecia dose range

15-30 mg

Regeneron price target (RBC)

$707
$ABBV$MRNA$LLY$PFE$REGN

AbbVie ($ABBV) announced that the European Medicines Agency's Committee for Medicinal Products for Human Use (CHMP) adopted positive opinions recommending approval of upadacitinib (RINVOQ) at 15 mg and 30 mg once daily for the treatment of adult and adolescent patients with severe alopecia areata, and at 15 mg once daily for non-segmental vitiligo. The final European Commission decision is expected in the coming months, with RINVOQ expected to be the first systemic medication for patients with non-segmental vitiligo if approved.

$MRNA shares have gained 125.51% year to date, driven by an FDA flu vaccine win, a corporate pivot, and an expanding pipeline. Eli Lilly ($LLY) has gained roughly 6% over the past 30 days, with the Street expecting more than 13.6% upside from current levels. Pfizer ($PFE) Chief International Commercial Officer Alexandre de Germay stated that China has moved ahead of Europe in pharmaceutical innovation and drug development, with China now accounting for 40% of all clinical studies in oncology globally.

Regeneron Pharmaceuticals ($REGN) announced that the FDA and the European Medicines Agency accepted regulatory applications for cemdisiran to treat adults with generalized myasthenia gravis who are anti-acetylcholine receptor antibody-positive. RBC Capital maintained a Sector Perform rating on $REGN with a $707 price target, though the firm noted that $ABBV's acquisition of Apogee Therapeutics is a net negative for the company.

MedTech & Devices

Neutral

Thermo Fisher microbiology sale

$1.075B
$DXCM$DHR$TMO

DexCom ($DXCM) announced that the FDA cleared growing use of its Stelo Glucose Biosensor beyond adults for children ages 2 and older who do not use insulin. President and CEO Jake Leach stated that glucose matters for everyone, and the company plans to broaden access to continuous glucose monitoring technology.

Masimo, a specialty diagnostics solutions innovator within Danaher Corporation ($DHR), announced FDA 510(k) clearance for an opioid-induced respiratory depression detection capability integrated into the Radius VSM wearable continuous patient monitor. Thermo Fisher Scientific ($TMO) completed a $1.075B sale of its microbiology business at a 1.7x sales multiple, which was noted as dilutive to earnings per share.

Health Insurance & Managed Care

Bullish

UnitedHealth 30-day gain

10%+10%
$UNH

UnitedHealth Group ($UNH) has gained more than 10% over the past 30 days and is now trading close to its 52-week high. The performance has been driven by positive analyst upgrades and a proposed FTC action, with Bank of America raising its price target on the stock while maintaining a Buy rating.

$JNJ

Johnson & Johnson ($JNJ) prevailed in a Los Angeles jury trial on June 6, with the jury finding that the company was not negligent in a lawsuit alleging its talc products led to ovarian cancer in three women. The verdict provides a legal win for $JNJ as it continues to defend against similar product liability claims related to its talc-based consumer products.

Looking Ahead

Neutral

Core PCE inflation

3.4%

S&P 500 futures

-0.3%-0.3%
$ABBV$REGN

The European Commission is expected to issue final decisions on $ABBV's upadacitinib applications for alopecia areata and non-segmental vitiligo in the coming months, following the positive CHMP opinions. Regulatory applications for $REGN's cemdisiran are now under review at both the FDA and European Medicines Agency for generalized myasthenia gravis. Broader healthcare equity performance may continue to face headwinds from persistent inflation, with core PCE inflation sitting at 3.4% year over year and E-mini S&P 500 futures down approximately 0.3%.

What to Watch

Coming months

European Commission decision on RINVOQ for alopecia areata and vitiligo

$ABBV
High

Risk Flags

WatchCore PCE inflation at 3.4% YoY keeps Fed cautious, pressuring healthcare equities
NoteChina accounting for 40% of global oncology trials shifts competitive landscape

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