Companies/Sector

Health Care

Pharma, biotech, medical devices, insurers and providers.

Sector today, equal-weighted−1.70%1 up · 9 down
CompanyPriceToday1 monthYTD
Amgen AMGN
Biotechnology
414.19▼ 0.86%+8.6%+5.2%
Eli Lilly LLY
Pharmaceuticals
1,161.67▼ 1.81%+2.2%+7.9%
Gilead Sciences GILD
Biopharmaceuticals
147.69▼ 1.96%+0.9%+9.6%
Hims & Hers Health HIMS
Digital health and telehealth
29.53▼ 3.43%+2.5%+43.0%
Intuitive Surgical ISRG
Surgical Robotics and Medical Devices
423.47▼ 0.88%+11.9%+2.0%
Johnson & Johnson JNJ
Pharmaceuticals and medical devices
248.77▼ 5.78%−6.6%−3.0%
Merck MRK
Pharmaceuticals
141.84▼ 2.64%−1.9%−4.9%
Moderna MRNA
Biotechnology
218.08▲ 2.41%+48.5%+31.1%
Novo Nordisk NVO
Pharmaceuticals
38.13▼ 1.36%−12.6%−12.9%
UnitedHealth Group UNH
Managed Health Care
379.54▼ 0.67%−1.2%+13.8%

News across the sector

J&J Q3 2026 sales rise 5.9% to $25.4B; raises reported sales guidance

Johnson & Johnson reported third-quarter 2026 worldwide sales of $25.4 billion, up 5.9%, and adjusted EPS of $2.59, down 7.5%.

Johnson & Johnson

UnitedHealth Q3 2026 adjusted EPS $4.69 vs $2.92 a year ago; 2026 adjusted EPS floor raised to $20.50

UnitedHealth reported third-quarter 2026 revenue of $112.7 billion, slightly below $113.2 billion a year earlier, and adjusted EPS of $4.69 against $2.92.

UnitedHealth Group

J&J declares $1.34 quarterly dividend for fourth quarter 2026

The Board of Directors declared a cash dividend of $1.34 per share for the fourth quarter of 2026, announced alongside the third-quarter results.

Johnson & Johnson

Johnson & Johnson files 8-K: Results of Operations (Item 2.02)

Johnson & Johnson filed a Form 8-K with the SEC on Oct 13, 2026, 8:12 AM ET, reporting an event dated Oct 13, 2026.

Johnson & Johnson

Novo Nordisk: 6-K filed (report of foreign private issuer)

A Form 6-K (report of foreign private issuer) relating to Novo Nordisk was filed with the SEC on Oct 13, 2026, 6:15 AM ET.

Novo Nordisk

UnitedHealth files 8-K: Results of Operations (Item 2.02)

UnitedHealth filed a Form 8-K with the SEC on Oct 13, 2026, 6:14 AM ET, reporting an event dated Oct 13, 2026.

UnitedHealth Group

Taltz plus Zepbound shows broader biomarker changes than Taltz alone in psoriasis

On October 9, 2026 Lilly reported exploratory biomarker data from the TOGETHER-PsO Phase 3b trial, presented at Fall Clinical Dermatology.

Eli Lilly

CMS releases 2027 Medicare Advantage Star Ratings; 71% of enrollees in 4-star-plus contracts

CMS published the 2027 Medicare Advantage and Part D Star Ratings on October 8, 2026.

Medicare Advantage

Hims & Hers files 8-K: Director/Officer Change

Hims & Hers filed a Form 8-K with the SEC on Oct 7, 2026, 4:13 PM ET, reporting an event dated Oct 7, 2026.

Hims & Hers Health

Dutch court finds Keytruda SC infringes Halozyme patent, barring sales in eight European countries

A Dutch patent court found that Merck's subcutaneous Keytruda infringes Halozyme's EP 2,797,622 patent and rejected Merck's argument that the patent is invalid.

Merck

Novo Nordisk: 6-K filed (report of foreign private issuer)

A Form 6-K (report of foreign private issuer) relating to Novo Nordisk was filed with the SEC on Oct 6, 2026, 8:11 AM ET.

Novo Nordisk

Lilly presents 21 dermatology presentations at Fall Clinical 2026

Lilly announced on October 5, 2026 that it would present 21 dermatology presentations at the Fall Clinical Dermatology Conference in Las Vegas, held October 8-11.

Eli Lilly

Novo Nordisk: 6-K filed (report of foreign private issuer)

A Form 6-K (report of foreign private issuer) relating to Novo Nordisk was filed with the SEC on Oct 2, 2026, 5:53 PM ET.

Novo Nordisk

FDA approves Jaypirca as first-line treatment for untreated CLL/SLL

The FDA approved Jaypirca (pirtobrutinib) on October 2, 2026 as a first-line treatment for adults with previously untreated CLL or SLL who do not have a 17p deletion.

Jaypirca

FDA extends review of denecimig haemophilia A BLA over manufacturing remediation

The FDA is still reviewing Novo's biologics license application for denecimig, a haemophilia A treatment, and has set no new decision date.

Rare disease