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Stocks tumbled as sweeping tax and spending bill could dramatically increase federal deficit

SOTIO Biotech

15/8/2025 | 3 minuty čtení

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US court has ruled that President Trump overstepped his authority when imposing his tariffs. But an appeals court later suspended the earlier judgment. Stocks also tumbled as investors kept close tabs on a sweeping tax and spending bill that could dramatically increase the federal deficit.

Monthly market moves of selected competitors compared to NASDAQ Biotechnology Index (NBI)

Monthly market moves of selected competitors compared to NASDAQ Biotechnology Index (NBI)

Area

Company

Ticker

Price range $

Δ  Price

MktCap $m

Δ MktCap $m

ADC

ADC Therapeutics

ADCT

1.27 – 3.09

116

%

306

164

Elevation Oncology

ELEV

0.28 – 0.36

-19

%

18

-4

Mersana Therapeutics

MRSN

0.31 – 0.40

-21

%

42

-12

Sutro Biopharma

STRO

0.73 – 1.10

-14

%

75

-13

IL15 / 2

ImmunityBio

IBRX

1.89 – 2.90

6

%

2 271

128

Mural Oncology

MURA

2.51 – 2.98

0

%

45

0

Nektar Therapeutics

NKTR

0.59 – 0.78

-9

%

134

-14

Werewolf Therapeutics

HOWL

0.80 – 1.28

34

%

54

14

CAR-T

Allogene Therapeutics

ALLO

0.95 – 1.70

-30

%

254

-111

Arcellx

ACLX

52.80 – 65.55

-4

%

3 410

-159

Autolus Therapeutics

AUTL

1.18 – 1.75

24

%

466

90

Mustang Bio

MBIO

1.09 – 1.34

20

%

4

1

Other

Arcus Biosciences

RCUS

8.01 – 9.51

2

%

945

19

Immutep

IMMP

1.67 – 2.49

10

%

274

25

MacroGenics

MGNX

1.36 – 1.75

-22

%

86

-24

ADC Therapeutics

ADCT announced further positive data for Zynlonta, a CD19-directed ADC, in combination with Roche’s Columvi (glofitamab) from the Phase 1b LOTIS-7 trial. The new data shows the combination had a 95.5% ORR and 90.9% CR rate in 22 patients with relapsed or refractory DLBCL. The company separately announced that it has terminated the development of ADCT-602, which was in a Phase 1/2 trial in patients with relapsed or refractory B-cell ALL.

Elevation Oncology

Elevation reported net loss for 1Q 2025 of $14 million, compared to $11 million for 1Q 2024. The company also confirmed discontinuation of development of EO-3021 and implementation of a workforce reduction of approximately 70%.

Mersana Therapeutics

Mersana announced the implementation of a strategic restructuring and reprioritization plan aimed at extending the company’s cash runway and furthering the development of emiltatug ledadotin, a B7-H4-directed Dolasynthen ADC.

Sutro Biopharma

Sutro announced in its financial results that net loss for 1Q 2025 was $76 million, compared to $58 million for 1Q 2024.

ImmunityBio

ImmunityBio achieved net product revenue of approximately $17 million, representing a 129% increase over $7 million in Q4 2024. Anktiva unit sales volume in Q1 2025 grew 150% over Q4 2024, with monthly volume in March up 69% over February.

Mural Oncology

Short interest of Mural increased by 18 % to 657,864 reported on May 15, compared to 562,784 on April 15.

Nektar Therapeutics

Nektar reported net loss for 1Q 2025 of $51 million, or $0.24 per share, as compared to a net loss of $37 million, or $0.19 per share, in 1Q 2024.

Werewolf Therapeutics

Werewolf announced in its quarterly financial results that net loss was $18 million for the first quarter of 2025, compared to $16 million for the same period in 2024. The company also said that WTX-124 Phase 1/1b trial is on track for data readouts and interactions with the FDA in the second half of the year.

Allogene Therapeutics

Allogene reported a net loss for the first quarter of 2025 of $60 million, or $0.28 per share. The company also announced it will hold an oral presentation of ALLO-316 in kidney cancer and ALPHA3 TIP poster for cema-cel at ASCO Meeting.

Autolus Therapeutics

recommended European Commission approval of obe-cel for the treatment of adult patients, 26+, with relapsed or refractory B-cell precursor ALL. Separately, the company announced a net loss of $70 million for 1Q 2025, compared to $53 million for the same period in 2024.

Arcellx

Arcellx announced new positive data for its iMMagine-1 study in patients with relapsed and/or refractory multiple myeloma. Results from all 117 patients dosed in the pivotal Phase 2 iMMagine-1 study of anito-cel demonstrated 97% ORR and 68% CR/sCR at a median follow-up of 12.6 months. No delayed neurotoxicities including no Parkinsonism, no cranial nerve palsies, and no Guillain-Barré syndrome, and no immune-mediated enterocolitis have been observed to date with anito-cel. The data were presented during an oral presentation at EHA 2025.

Mustang Bio

Short interest of Mustang dropped by 70 % to 58,835 reported on May 15, compared to 199,322 on April 30.

Immutep

Immutep announced that the investigator-initiated EFTISARC-NEO Phase 2 trial evaluating efti with radiotherapy plus Keytruda in the neoadjuvant setting for resectable soft tissue sarcoma (STS) has met its primary endpoint. The novel combination significantly exceeded the study’s prespecified median of 35 % tumor hyalinization/fibrosis versus 15 % for historical data from radiotherapy alone in patients with resectable STS.

MacroGenics

MacroGenics reported in its quarterly financial results that a net loss was $41 million for 1Q 2025, compared to a net loss of $52 million for 1Q 2024.

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